Introduction Following the detection of fetal growth restriction, there is no consensus about the criteria that should trigger delivery in the late preterm period. The consequences of inappropriate early or late delivery are potentially important yet practice varies widely around the world, with abnormal findings from fetal heart rate monitoring invariably leading to delivery. Indices derived from fetal cerebral Doppler examination may guide such decisions although there are few studies in this area. We propose a randomised, controlled trial to establish the optimum method of timing delivery between 32 weeks and 36 weeks 6 days of gestation. We hypothesise that delivery on evidence of cerebral blood flow redistribution reduces a composite of perinatal poor outcome, death and short-term hypoxia-related morbidity, with no worsening of neurodevelopmental outcome at 2 years.
Methods and analysis Women with non-anomalous singleton pregnancies 32+0 to 36+6 weeks of gestation in whom the estimated fetal weight or abdominal circumference is <10th percentile or has decreased by 50 percentiles since 18–32 weeks will be included for observational data collection. Participants will be randomised if cerebral blood flow redistribution is identified, based on umbilical to middle cerebral artery pulsatility index ratio values. Computerised cardiotocography (cCTG) must show normal fetal heart rate short term variation (≥4.5 msec) and absence of decelerations at randomisation. Randomisation will be 1:1 to immediate delivery or delayed delivery (based on cCTG abnormalities or other worsening fetal condition). The primary outcome is poor condition at birth and/or fetal or neonatal death and/or major neonatal morbidity, the secondary non-inferiority outcome is 2-year infant general health and neurodevelopmental outcome based on the Parent Report of Children’s Abilities-Revised questionnaire.
Ethics and dissemination The Study Coordination Centre has obtained approval from London-Riverside Research Ethics Committee (REC) and Health Regulatory Authority (HRA). Publication will be in line with NIHR Open Access policy.
Trial registration number Main sponsor: Imperial College London, Reference: 19QC5491. Funders: NIHR HTA, Reference: 127 976. Study coordination centre: Imperial College Healthcare NHS Trust, Du Cane Road, London, W12 0HS with Centre for Trials Research, College of Biomedical & Life Sciences, Cardiff University. IRAS Project ID: 266 400. REC reference: 20/LO/0031. ISRCTN registry: 76 016 200.
- fetal medicine
- maternal medicine
This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Strengths and limitations of this study
Changes in cerebral Doppler measures are considered a strong candidate for triggering delivery following detection of late preterm fetal growth restriction.
The primary outcome is a composite of perinatal and neonatal outcome, and infants will be followed to determine health and neurodevelopment at 2 years to ensure safety and non-inferiority of intervention.
This appropriately powered UK and European multicentre trial will inform NHS policy and the findings will be generalisable to late preterm fetal growth restriction in other healthcare systems.
There are limited data available in respect of selecting the threshold of cerebral Doppler change for randomisation.
Some non-UK centres will not randomise women at the earlier gestation range (32–33+6 weeks) and this could limit the generalisability of the results in this group of women.
Third trimester poor fetal growth and compromise are strongly associated with stillbirth, neonatal illness1 and an increased risk of fetal or neonatal brain injury.2 The only therapeutic option is delivery of the fetus. This poses a dilemma: delivery too early may incur the complications of prematurity, delivery too late risks further fetal compromise, brain injury and late stillbirth. The problem of when to deliver these babies is twofold: there is no consensus on how to identify fetal compromise and there is no ‘ideal’ evidence-based monitoring strategy. Current screening strategies include standardised symphysis-fundal height measurement, third trimester ultrasound and umbilical Doppler velocimetry.3 4 National Institute for Health and Care Excellence (NICE) acknowledges that methods to identify fetal growth restriction (FGR) are ‘poorly developed or not tested by rigorous methodology’.
The use of Doppler ultrasound of fetal vessels allows non-invasive assessment of blood flow. Fetal ‘cerebral blood flow redistribution’, prioritising blood flow toward the brain at the expense of other organs, is a response to an adverse intrauterine environment characterised by hypoxaemia. Ultrasound markers of such fetal compromise include Doppler assessment of blood flow velocity5–7 and abdominal circumference growth velocity ‘drop off’ in the third trimester.8 9 Intervention by delivery of the fetus in response to either evidence of blood flow redistribution or fetal growth slowing has never been tested in a randomised trial. Computerised cardiotocography (cCTG) has been used in several observational studies to determine fetal condition in relation to hypoxaemia and acidosis. The RCOG (Royal College of Obstetricians and Gynaecologists) recommends that research is required to evaluate the effectiveness of third trimester ultrasound assessment, concluding that ‘middle cerebral artery (MCA) Doppler may be a more useful test in small for gestational age (SGA) fetuses detected after 32 weeks’4 but does not define parameters that should trigger delivery. Even with effective screening for FGR, the questions of how to monitor and when to deliver would remain.
A Cochrane review of the management of ‘compromised babies’ at term showed no difference in perinatal or long-term outcome with a policy of early delivery versus conservative management.10 Only three trials were included: two included small babies, both part of the DIGITAT (Disproportionate Intrauterine Growth Intervention Trial At Term) study (a small pilot and the main trial),11 the third included babies with reduced amniotic fluid. There is no Cochrane review on the optimal timing of delivery in late preterm growth restricted babies.
A systematic review included only one trial of timed delivery in late preterm babies. The Growth Restriction Intervention Trial12 included 547 babies from 24 to 36 weeks of gestation with evidence of preterm growth restriction or compromise, where there was clinical uncertainty whether immediate delivery was indicated. Of these, 210 babies were recruited between 33+0 and 36+6 weeks: 107 women were randomised to early delivery and 103 to delayed delivery. Mortality and a range of neurodevelopmental measures were similar between the groups. These results cannot be used to inform management because of the small number of infants assessed using only umbilical artery Doppler velocimetry, the subjective assessment of the cardiotocograph (ie, not computerised analysis), and the use of clinician’s discretion rather than standardised management.
Results from our previous randomised trial of delivery decision-making using Doppler velocimetry and cCTG in pregnancies with FGR at 26–32 weeks of gestation—the TRial of Umbilical Fetal FLow in Europe (TRUFFLE) provided evidence associating monitoring strategies with improved outcomes13 and guides practice internationally.14 15 In TRUFFLE (2005–2010) we studied FGR <32 weeks of gestation using cCTG as the standard of care for timing delivery, compared with early or late fetal ductus venosus (DV) Doppler velocimetry changes with a cCTG ‘safety net’. Surviving infants whose mothers had been randomised to delivery in late DV changes arm showed better neurodevelopment at 2 years of age.13
We then carried out the prospective multicentre observational TRUFFLE 2 Feasibility Study (2017–2018, n=1024). A range of markers of cerebral redistribution were evaluated as potential delivery trigger points in two gestational age bands. These included the MCA Doppler and the umbilical cerebral ratio (UCR); calculated by dividing the Doppler pulsatility index of the umbilical artery by that of the MCA. Participating clinicians suggested greater concern about fetal condition is required to trigger delivery at earlier rather than later gestational ages between 32 and 36 weeks. We, therefore, selected a more abnormal threshold for cerebral redistribution at earlier gestational ages, based on stepped UCR z-score values.16 Of note was the finding from a prospective study that birth condition, fetal mortality and neonatal morbidity rate were more common among fetuses showing higher UCR z-score, indicating cerebral redistribution, compared with those with a lower UCR z-score (15 vs 9%).17
On this basis, we designed this randomised trial of delivery for women identified with late preterm FGR, to test the hypothesis that delivery based on UCR values derived from the feasibility study will safely lead to improved fetal outcomes (TRUFFLE 2).
Methods and analysis
This is an individual unblinded randomised trial of pregnant women experiencing FGR. Following informed consent, 1560 women will be randomised to either immediate or delayed delivery. Women are being recruited from UK and European centres.
Potential participants are women with singleton non-anomalous pregnancies between 32+0 and 36+6 weeks of gestation in whom a SGA fetus is identified or one whose growth has slowed. This is defined as estimated fetal weight or abdominal circumference <10th percentile and/or having decreased by 50 percentiles since an ultrasound scan at 18–32 weeks. Biometry must have been performed in the 14 days prior to inclusion. Each centre will use local growth charts. Data is collected on absolute measurements and growth chart-derived percentiles. Once identified as potential participants women receive regular monitoring as per local standard of care for fetal condition, using ultrasound biometry, umbilical and MCA Doppler velocimetry assessments and cCTG (using Dawes-Redman criteria). This is recommended to be repeated every 14 days; these observational data are recorded.
Women become eligible for randomisation when signs of fetal cerebral blood flow redistribution are detected by Doppler, defined below and shown in the study flow chart (online supplemental file 1—flow chart).
Delivery is based on UCR pulsatility index z-scores, of >1.5 (between 32+0 and 33+6 weeks) or >1.0 (34+0 to 36+6 weeks). These correspond to an absolute UCR of ≥1.0 at 32+0 to 33+6 weeks and ≥0.8 at 34+0 to 36+6 weeks. Abnormal UCR measurements must be repeated within 15 minutes–24 hours to confirm these values. This need not be consecutive, so that if the second measurement is normal the patient may still be randomised if a repeat Doppler measurement is abnormal within 72 hours of the first abnormal measurement. Randomisation will occur at the time of the second qualifying UCR measurement and is stratified by centre and gestational age. Randomisation is through the CASTOR website (Amsterdam, NL) into which eligibility, monitoring and outcome data are entered.
Women are consented in a two-stage process. Stage 1 (pre-eligible) consent is not a prerequisite and women may be consented directly for randomisation with stage 2 (eligible for randomisation) consent.
Pre-eligible: consent for observational data collection
Consented for prospective data collection once identified as meeting criteria for SGA or slowed fetal growth (as defined above) but not meeting cerebral Doppler thresholds for randomisation or not willing to be randomised. This will include demographics, medical history, ultrasound findings and outcomes. This consent will include obtaining a personal email address, which is entered into and stored on Castor, and willingness to be contacted in the future for follow-up where women are randomised (online supplemental file 2—consent form for observational data collection).
Eligible for randomisation: consent for randomisation
Consent for randomisation once cerebral redistribution is identified, with UCR (as defined above) of ≥1.0 at 32+0 to 33+6 weeks and ≥0.8 at 34+0 to 36+6 weeks. This consent will also include contact details and willingness to be contacted in the future for follow-up data collection (online supplemental file 3—consent for randomisation).
Women are randomly allocated to either immediate delivery or delayed delivery as defined below. Randomisation has a 1:1 allocation ratio and stratified based on gestational age (above or below 34 weeks) and centre. Randomisation is conducted on the electronic data capture platform (Castor EDC, Amsterdam, The Netherlands).
Participants in the immediate delivery arm will be delivered by Caesarean or induction of labour will be commenced within 48 hours, allowing for administration of corticosteroids and infusion of magnesium sulphate as per local protocol and guidance. Start of induction of labour is defined as administering cervical preparation (cervical balloon, prostaglandins, etc), artificial rupture of membranes or administration of oxytocin.
Participants in the delayed delivery arm will be monitored using twice weekly Doppler and cCTG monitoring, or more frequently based on local clinical protocols if required. Umbilical artery Doppler velocities may be measured in this time and delivery may be based on these safety net criteria (see box below). We strongly recommend that MCA measurements are not undertaken during monitoring in the delayed delivery arm. Delivery is indicated when short term variation (STV) is <4.5 ms on cCTG or there are repeated fetal heart rate decelerations. Once participants reach 37+0 weeks of gestation the delivery plan will be based on local protocols.
Delivery thresholds based on umbilical artery Doppler for participants in all arms of the study
Umbilical Doppler delivery thresholds.
In all arms absolute indications for delivery include:
Umbilical artery Doppler with reversed end diastolic flow after entry into the trial, OR
Umbilical artery Doppler absent end diastolic flow from 34+0 weeks.
Study setup: 0–10 months; recruitment/randomisation: 11–36 months. Two years follow-up questionnaires 35–60 months; analyses, writing up, reporting and dissemination: 61–66 months. This equates to 5 and ½ years (66 months).
Study outcome measures
The primary outcome for the study is a composite of fetal or infant death, composite measure of poor condition at birth and neonatal morbidity—as defined by presence of any of the following:
Poor condition at birth
Apgar score at 5 min <7, umbilical artery pH <7.0 or umbilical vein pH <7.1.
Need for resuscitation with intubation, chest compressions or medication.
Fetal death/ death before neonatal hospital discharge
Neonatal brain injury syndromes
Infants with a diagnosis consistent with hypoxic ischaemic encephalopathy (HIE): term and near-term infants only.
Infants with a diagnosis of intracranial haemorrhage, perinatal stroke, HIE, central nervous system infection, or kernicterus (bilirubin encephalopathy): all infants.
Preterm white matter disease (periventricular leukomalacia): preterm infants only.
Infants with a recorded seizure confirmed by Electro-encephalogram (EEG).
Need for mechanical support of respiration after admission to neonatal unit (NNU), for more than 1 hour; includes need for continuous positive airways pressure (or NIPPV; Noninvasive positive-pressure ventilation) or mechanical ventilation via endotracheal tube but excludes need for supplemental oxygen.
Hypotensive treatment, patent ductus arteriosus requiring treatment, or disseminated coagulopathy.
Clinical sepsis with positive blood culture.
necrotising enterocolitis requiring surgery.
Retinopathy of prematurity requiring treatment (laser or anti Vascular Endothelial Growth Factor (VEGF) injections)
For the baby
Health and developmental outcomes—assessed using Parent Report of Children’s Abilities-Revised (PARCA-R) questionnaire at 2 years corrected age and an Infant Health Questionnaire up to 2 years (online supplemental file 4—PARCA-R Questionnaire and online supplemental file 5—Infant Health Questionaire).
The PARCA-R18 will be completed at 24 months term-equivalent age, this allows derivation of the non-verbal cognitive scale and language development scale. Raw scores from the scales are standardised (by corrected age and gender) to a notional population mean of 100 (SD=15) and the average of these two component scores will be taken as the overall composite score. Corrected age is used for preterm babies (born before 37 weeks) and represents the age of the child from the estimated date of delivery.
The Infant Health Questionnaire19 will be used to derive the following health outcomes at 6, 12, 18 and 24 months post partum:
Use of any hospital service (yes/no) and total number of contacts over the 2-year period.
Admitted to hospital (yes/no) and total number of admissions over the 2-year period.
Planned/unplanned admissions to hospital (yes/no) over the 2-year period.
Intensive care or not over the 2-year period.
Attended emergency department (and not subsequently admitted) (yes/no) over the 2-year period.
Attended Outpatients/clinic (yes/no) over the 2-year period.
For the mother
Gestational hypertension developed post study entry
As defined by the International Society for Study of Hypertension in pregnancy (ISSHP):20 hypertension (blood pressure ≥140/90 mm Hg) arising de novo after 20 weeks gestation in the absence of proteinuria.
Pre-eclampsia developed post study entry
As defined by the ISSHP:20 blood pressure ≥140/90 mm Hg and significant proteinuria (protein/creatinine ratio of 30 mg/mmol or more).
Onset of labour (spontaneous, induction (method), prelabour caesarean section).
Mode of delivery (spontaneous vaginal, assisted vaginal, caesarean section).
Doppler quality control
Each sonographer in each centre taking part in the trial are assessed by the local principal investigator (PI). Each sonographer will submit to the local PI two images: pseudo anonymised ultrasound images for each Doppler parameter (umbilical artery and MCA) each showing a colour Doppler image with the gate placed over the vessel, and the pulsed wave Doppler waveform arising from that image. The local PI will determine whether these images are satisfactory using a predefined quality control scoring system (online supplemental file 6—Doppler image scoring sheet).
Doppler ultrasound criteria
Measurements are obtained in fetuses between 32+0 and 36+6 weeks of gestation. Umbilical artery and MCA pulsatility index images are collected according to specific predefined objective criteria for both the colour Doppler images and pulsed wave Doppler.
Doppler quality control
The local PI will provide details of all sonographers having undergone standardisation in that centre to the Centre for Trials Research (CTR). The CTR will independently request all images submitted to the local PI for the first five patients randomised from each unit, and then for up to 10% of patients thereafter, for anonymised quality control assessment by the Quality Control Board. All images are collected as pseudo anonymised .jpeg images and saved electronically in a Doppler ultrasound sonographer standardisation file by the PI, with the submitting sonographer identifiable. Images are scored using the predefined scoring criteria. The CTR will manage this process and will provide feedback if necessary, and ensure that members of the TRUFFLE 2 Quality Control Board do not assess images from their own unit.
Ultrasound scan of fetal growth between 30+0 and 36+6 weeks of gestation, including measurement of MCA and umbilical artery Doppler velocities.
cCTG STV analysed using Dawes-Redman criteria.
(All criteria should be fulfilled to be eligible for randomisation)
Women ≥18 years old.
Pregnant with singleton non-anomalous fetus.
Between 32+0 and 36+6 weeks of gestation.
Estimated fetal weight or abdominal circumference <10 th percentile OR decreased by 50 percentiles since an ultrasound scan at 18+0–32+0 weeks.
Cerebral redistribution defined as UCR ≥1.0 (between 32+0 and 33+6 weeks) or ≥0.8 (34+0 to 36+6 weeks) repeated within 15 minutes–24 hours.
Normal STV on cCTG (4.5 msec or above).
Indication for immediate delivery required within 48 hours.
Unable to give informed consent.
Preterm prelabour rupture of the membranes.
Suspected placental abruption or antepartum haemorrhage.
Presence of reversed end diastolic flow in the umbilical artery.
Assessment and follow-up
Assessment of the primary outcome is at infant discharge from the NNU and assessment of the key secondary infant outcomes will use the Infant Health Questionnaire and PARCA-R. The Infant Health Questionnaire will be sent out by investigators via Castor at 6, 12, 18 and 24 months post partum. Neurodevelopment is assessed at 2 years age corrected for prematurity using the PARCA-R, also sent via Castor (translated into local language). The window for determining 2-year outcome is from 23.5 to 27.5 months over which range the PARCA-R has been standardised.
Endpoint is 30 months after the estimated date of delivery of the last participant to deliver (24 months follow-up with additional 6 months for data cleaning and additional enquiries).
Statistics and data analysis
The trial is powered to detect if immediate delivery following cerebral redistribution is superior to expectant management following cerebral redistribution on this outcome. A difference in the proportion with the primary outcome from 15% in the delayed delivery to 9% in the immediate delivery (from TRUFFLE 2 feasibility study) demonstrates an OR of 0.56. At two-sided 5% significance with 95% power, 780 participants per arm are required, giving 1560 in total. Given the immediacy of this outcome, no loss to follow-up is expected. An important non-inferiority secondary safety outcome is infant neurodevelopment, which is measured by parent completed questionnaire at 2 years using the PARCA-R, as recommended in NICE Guidance,21 supplemented by infant health information over the intervening 2 years. Assuming a loss to follow-up at 2 years of 20%, 2-year outcomes for approximately 1248 infants are expected (624 per group assuming no difference in the lost to follow-up between the groups). The PARCA-R questionnaire provides a composite score for neurodevelopment with a standardised mean of 100 and SD of 15. With a one-sided significance level of 1%, under a non-inferiority hypothesis, a sample size of 624 in each group achieves a 98% power to detect a non-inferiority margin of difference in the mean PARCA-R score of no less than four points (0.25 of a SD). A margin of no less than three points can be detected with 90% power.
The primary analysis approach for the primary outcome of composite of adverse fetal/neonatal outcomes, maternal secondary outcomes and the Infant Health Questionnaire will be intention to treat with participants analysed in the groups to which they are assigned regardless of deviation from the protocol or intervention received. The PARCA-R will be both an intention to treat and a per protocol analysis, since the hypothesis under examination for these outcomes is a non-inferiority hypothesis. The per-protocol analysis will exclude babies of women who do not receive their intervention as planned. As the trial includes multiple centres (and will involve a reasonable number of participants randomised per centre), the analysis will be based on the individual participant, allowing for clustering between participants within centre using robust SEs. All analyses will additionally adjust for gestational age at inclusion (stratification risk factor used in randomisation) as a fixed factor. For binary outcomes (composite of adverse fetal/neonatal outcomes, gestational hypertension, pre-eclampsia) a logistic regression model will be used to compare this outcome by arm and results presented as ORs and two-sided 95% CI. Continuous outcomes (PARCA-R, Infant Health Questionnaire) will be analysed using linear regression and results presented as adjusted differences in means alongside 95% CIs. The Infant Health Questionnaire will also be examined over time using a repeated measures model, and will include an interaction term for time (6, 12, 18 and 24 months) and trial arm to investigate any divergent or convergent pattern in Infant Health Questionnaire. The categorical outcomes of mode of delivery and onset of labour will be compared between trial arms by fitting a multilevel ordinal regression model. The neonatal secondary outcome will be examined using the mean PARCA-R score between each trial arm using linear regression, and a one-sided 95% CI constructed to assess non-inferiority. Additional pre-specified sub-group analyses will be carried out to analyse the primary outcome in the whole cohort by those that are <10th percentile (vs ≥10th) and <3rd percentile (vs ≥3rd) based on different growth charts, maternal morbidity (yes/no) and corticosteroid administration (yes/no).22 23 If numbers are sufficient, we will also describe the intervention effect in the subgroups <3rd percentile versus 4–10th vs >10th percentile but will not statistically test for intervention effect.
All analyses will be undertaken after database lock following data collection at 2 years. No interim analyses are planned. Missing outcome data but will be accounted for in sensitivity analyses using multiple imputation, where we will assume that outcome data are missing at random given the observed measurements. All planned analyses will be described in detail in a statistical analysis plan, which will be finalised prior to database lock. The reporting of findings will be in accordance with the Consolidated Standards of Reporting Trials guidelines for Randomized Controlled Trials (RCTs). Statistical analysis will be performed in Stata (V.16 or higher).
Data collection and randomisation are carried out on a secure cloud-based electronic data capture platform (Castor EDC, Amsterdam, The Netherlands). Participants can only be identified by their recruiting centres using unique trial identifiers. Participant email addresses will be stored for sending follow-up questionnaires within an encrypted section of Castor only their recruiting centre has access to.
A Trial Management Group will meet monthly to review study progress and recruitment targets. In addition there will be a Trial Steering Committee and Data Monitoring Committee, with a majority of independent members, to guarantee the safety of study participants.
A clinical trial risk assessment has been developed by CTR at Cardiff University, to determine the intensity and focus of central and on-site monitoring activity in the TRUFFLE 2 trial. Appropriate monitoring levels will be employed and are fully documented in the trial monitoring plan. Investigators should agree to allow trial related monitoring, including audits and regulatory inspections, by providing direct access to source data/documents as required. Findings generated from on-site and central monitoring will be shared with the Sponsor, Chief Investigator (CI), PI and local Research & Development (R&D) departments.
Serious adverse events (SAEs) will be reported for randomised participants and their infants. The reporting period is from the point of randomisation until discharge home for the mother and neonate, maternal death is to be reported up to 42 days after delivery. SAEs will be reported on the data capture platform (Castor) in accordance with the UK policy framework for Health and Social care research.
Patient and public involvement
Patient and public involvement (PPI) has been embedded throughout the development of this study.
SANDS, the Stillbirth and Neonatal Death charity in the UK, has been closely involved in the development and design of this study. SANDS is clear that there is an urgent need for better assessment and care of women and their babies in late pregnancy and are fully supportive of the study. They will play an integral role throughout the study and in publicising the study and disseminating results in accessible formats. The research and development lead at SANDS is a member of the Trial Management Group. In their role, they represent members of the public affected by stillbirth and neonatal death.
An FGR PPI panel was convened to discuss TRUFFLE 2 study design. The purpose of the workshop was to ask members of the public for their views on the study, with specific focus on the concept of randomisation, the current situation for the treatment of FGR, and the scope of this study. The FGR panel comprised eight women who had experienced FGR, stillbirth or uncomplicated pregnancies. At the workshop the proposed study design was discussed. Following the workshop, the women were asked to complete an anonymous questionnaire relating to early delivery compared with monitoring the health of the baby in the womb and randomisation. Overall, women were supportive of the study, one stated ‘I believe a lot of women will benefit from this study’. Another stated ‘The study will have an impact; it will act as a ripple effect on the family and wider public for the better.’ Regarding randomisation, most women said that they would be happy to be randomised to either arm while acknowledging that they would need support, one woman stated ‘Yes, I would be randomised but would need the right support from the clinical staff. I would need to have 100% trust in my doctors’. Two women from this panel have agreed to be involved in the management of the study as independent members of the Trial Steering Committee. We incorporated the views and feedback of the PPI panel in the drafting of the patient information leaflet and consent forms to ensure clarity and comprehensibility.
Ethics and dissemination
This protocol was written in accordance with the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) 2013 Statement (see online supplemental file 7—SPIRIT Checklist). The Study Coordination Centre has obtained approval from the London-Riverside Research Ethics Committee (REC) and Health Regulatory Authority (HRA). The study must also receive confirmation of capacity and capability from each participating NHS Trust before accepting participants into the study or any research activity is carried out. The study has also been submitted to research ethics committees in all participating countries, and each centre must confirm local ethical and hospital approval before starting recruitment. The study will be conducted in accordance with the recommendations for physicians involved in research on human subjects adopted by the 18th World Medical Assembly, Declaration of Helsinki 1964 and later revisions. Publication will be in line with National Institutes of Health Research (NIHR) Open Access policy.
Patient consent for publication
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Collaborators TRUFFLE 2 Investigators Group: Abin Thomas (Centre for Trials Research, Cardiff University, UK), Andrea Smith (Imperial College London, UK), Andrew Sharp (Harris-Wellbeing Preterm Birth Centre, University of Liverpool, UK), Andy Simm (Department of Diabetes and Endocrinology, Nottingham City Hospital, Nottingham, UK), Angela Ramoni (Department of Obstetrics and Gynecology, Medical University of Innsbruck, Austria), Barry Lloyd(Centre for Trials Research, Cardiff University, UK), Bianca Masturzo (Città della Salute e della Scienza, Turin, Italy), Christine Morfeld (Diakoniekrankenhaus Henriettenstiftung, Perinatalzentrum Hannover, Hannover, Germany), Christoph Brezinka (University of Innsbruck, Austria), Christopher Lloyd (Centre for Trials Research, Cardiff University, Cardiff, UK), Claudia Seidig (Perinatalzentrum, Hannover, Germany), Danielle Thornton (Imperial College London, Obstetrics and Gynaecology, Queen Charlotte's & Chelsea Hospital, London, UK), Elena Mantovani (Sezione di Ostetricia e Ginecologia, Dipartimento di Scienze della Vita e della Riproduzione, Università degli Studi di Verona, Verona, Italy), Emanuela Taricco (Department of Woman, Mother and Child, Buzzi Hospital, University of Milan, Italy), Emma Bertucci (Department of Medical and Surgical Sciences for Mothers, Children and Adults, University of Modena and Reggio Emilia, Azienda Ospedaliero Universitaria Policlinico, Modena, Italy, Erich Cosmi (Department of Woman' and Child's Health, University of Padova, Italy), Ferenc Macsali (Department of Obstetrics and Gynecology, Haukeland University Hospital, Bergen, Norway), Francesca Ferrari (Obstetrics & Gynecology, Policlinico University Hospital of Modena, Modena, Italy), Francesco D'Antonio (Centre for High Risk Pregnancy and Fetal Care, University of Chieti, Department of Obstetrics and Gynaecology, Chieti, Italy), Giuseppe Cali (Department of Obstetrics and Gynecology, Azienda Ospedaliera Villa Sofia Cervello, Palermo, Italy), Giuseppe Rizzo (Division of Maternal Fetal Medicine, Università di Roma Tor Vergata, Ospedale Cristo Re Roma, Rome, Italy), Ilaria Giuditta Ramezzana (Gynaecology and Obstetrics Unit, Department of Women's and Children's Health, Fondazione Ospedale Maggiore, Via Francesco Sforza 35, Milan 20122, Italy), Ioannis Kyvernitakis (Asklepios Hospital Barmbek, Hamburg, Germany), Karen Melchiorre (Department of Obstetrics and Gynecology, Spirito Santo Hospital of Pescara, Pescara, Italy), Kristiina Rull (Department of Obstetrics and Gynaecology, University of Tartu, Tartu, Estonia), Laura Sarno (Department of Neurosciences, Reproductive and Dentistry Sciences, University of Naples ‘Federico II’, Naples, Italy), Ligita Jokubkiene (Mälmo Department of Obstetrics and Gynecology, Skåne University Hospital, Lund University, Mälmo, Sweden), Liina Rajasalu (East Tallinn Central Hospital, Tallinn, Estonia), Louisa Jones (Imperial College London, Obstetrics and Gynaecology, Queen Charlotte's & Chelsea Hospital, London, London, UK), Makrina Savvidou (Chelsea and Westminster Hospital, Imperial College London, London, UK), Maria Stefopoulou (Center for Fetal Medicine Karolinska, University Hospital, Stockholm, Sweden), Mark Kilby (Birmingham Women's and Children's Hospital, Birmingham, UK), Nicola Fratelli (Department of Obstetrics and Gynecology, ASST Spedali Civili di Brescia and University of Brescia, Brescia, Italy), Nishigandh Deole (Obstetrics & Gynaecology, East Suffolk and North Essex NHS Foundation Trust, Ipswich Hospital, UK), Petra Pateisky (Department of Obstetrics and Gynecology, Division of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Vienna, Austria), Pilar Palmrich (Department of Obstetrics and Gynecology, Division of Obstetrics and Feto-Maternal Medicine, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria), Ralf Schild (Diakoniekrankenhaus Henriettenstiftung, Perinatalzentrum Hannover, Hannover, Germany), Roland Devlieger (Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium), Sabina Ondrová (Department for Mother and Child Care, Third Faculty of Medicine, Charles University, Prague, Czech Republic), Sanne Gordijn (Department of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands), Sarah Gumpert (Klinik für Geburtshilfe und Pränatalmedizin, Universitätsklinikum Eppendorf, Hamburg, Germany), Serena Simeone (Department of Sciences for the Health of Women and Children, Azienda Ospedaliera Universitaria Careggi, Florence, Italy), Silvia Salvi (UOC di Patologia Ostetrica, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy), Silvia Visentin (Department of Woman and Child's Health, University of Padova, Padova, Italy), Sofia Amylidi-Mohr (Department of Obstetrics and Gynecology, Inselspital, University of Bern, Bern, Switzerland), Stefan Verlohren (Department of Obstetrics, Charité - Universitätsmedizin, Berlin, Germany), Tanja Groten (Department of Obstetrics, University Hospital Jena, Jena, Germany), Tatjana Radaelli (Department of Obstetrics and Gynecology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy), Tinne Mesens (Faculty of Medicine and Life Sciences, Hasselt University, Hasselt, Belgium), Tiziana Fanelli (Fetal Medicine Unit, Di Venere and Sarcone Hospitals, ASL, BA, Bari, Italy), Wessel Ganzevoort (Department of Obstetrics and Gynecology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands), Yvonne Heiman (Department of Obstetrics, Jena University Hospital, Jena, Germany), Zulfiya Khodzhaeva (National Medical Research Center for Obstetrics, Gynecology and Perinatology Named After Academician V.I. Kulakov of Ministry of Healthcare of Russian Federation, 117997, Moscow, Russia).
Contributors BM-F drafted and revised the protocol. BA, ABe, EB, ABh, CB, ACB, JB, PC, EC, IC, AD'A, CE, EF, TF, WG, KH, PK, LK, PL, SL, NM, KMa, GMM, FM, KMy, RN, FP, LR, JR, RKS, TS, JT, HV, GV and LW contributed intellectually to the development of the protocol and revised the draft protocol. EM, JG, CP and JT revised the draft protocol. RC-J wrote the statistical analysis plan. HW designed the data collection database, wrote the statistical analysis plan, contributed intellectually to the development of the protocol and revised the draft protocol. CCL initiated the collaborative project, led the development of the protocol and revised the draft protocol. All authors approved the final version for publication. All members of the TRUFFLE 2 Investigator Group collaborated on the study.
Funding This research was funded by the National Institute for Health Research (NIHR) (127976). CCL is supported by the NIHR Biomedical Research Centre (BRC) based at Imperial College Healthcare NHS Trust and Imperial College London. BM-F was supported by a Fellowship Grant from Imperial Health Charity and NIHR Imperial BRC (RFRFPrD1920/104).
Disclaimer The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care.
Competing interests All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coidisclosure.pdfanddeclare: no financial relationships with any organisations that might have an interest in the submitted work in the previous 3 years; no other relationships or activities that could appear to have influenced the submitted work.
Provenance and peer review Not commissioned; peer reviewed for ethical and funding approval prior to submission.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.