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Do protocols for new randomised trials take previous similar trials into account? Cohort study of contemporary trial protocols
  1. Asger Sand Paludan-Müller1,
  2. Michelle C Ogden1,
  3. Mikkel Marquardsen1,
  4. Jonas Vive1,
  5. Karsten Juhl Jørgensen1,
  6. Peter Christian Gøtzsche1,2
  1. 1 Nordic Cochrane Centre, Rigshospitalet, Copenhagen, Denmark
  2. 2 Institute of Scientific Freedom, Copenhagen, Denmark
  1. Correspondence to Dr Peter Christian Gøtzsche; pcg{at}scientificfreedom.dk

Abstract

Objective To investigate to what extent evidence from previous similar trials or systematic reviews was considered before conducting new trials.

Design Cohort study of contemporary protocols for trials with ethical approval.

Methods All protocols for randomised trials approved by the five ethical committees in Denmark between January 2012 and March 2013 were screened for eligibility. Included protocols were read in full to determine whether a systematic search had been conducted and references were checked to evaluate whether trial rationale and design could be challenged for not adequately considering previous evidence. To investigate whether protocols cited relevant trials, we used simple search strategies that could easily be conducted by researchers without experience with literature searches.

Results Sixty-seven protocols were included. Only two (3%) of the protocols explicitly stated to have conducted a literature search and only one (1%) provided information that allowed the search to be replicated. Eleven (16%) of the protocols described trials where we found the information insufficient to judge if the trial was ethically justified, either due to a comparator that was not supported by the presented evidence (six protocols), because they did not present a rationale for conducting the trial (two protocols), or for both reasons (three protocols). For eight (12%) of the protocols, our search identified trials that could have been relevant to cite as justification.

Conclusions While most protocols seem to adequately consider existing evidence, a substantial minority of trials might lack a sufficient evidence base. Very few trials seemed to have been based on a literature search which makes it impossible to know whether all relevant previous trials had been considered. Rules for ethical approval should include requirements for systematic literature searches to ensure that research participants are not exposed to sub-optimal treatments or unnecessary harms as well as to reduce research waste.

  • medical ethics
  • clinical trials
  • statistics & research methods

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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Footnotes

  • Contributors PCG came up with the idea for the study and wrote the protocol. MCO, MM and ASPM collected data. MCO, ASPM and JV analysed the data. ASPM, JV, KJJ and PCG interpreted the data. ASPM wrote the first draft manuscript. All authors read and commented on the final manuscript.

  • Funding The study was funded by the Laura and John Arnold Foundation and the Nordic Cochrane Centre.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement No data are available.