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Sleeve gastrectomy versus Roux-en-Y gastric bypass for type 2 diabetes and morbid obesity: double-blind randomised clinical trial protocol
  1. Rinki Murphy1,
  2. Nicholas J Evennett2,
  3. Michael G Clarke2,
  4. Steven J Robinson2,
  5. Lee Humphreys2,
  6. Bronwen Jones2,
  7. David D Kim3,
  8. Richard Cutfield3,
  9. Lindsay D Plank4,
  10. Hisham Hammodat2,
  11. Michael W C Booth2
  1. 1Faculty of Medical and Health Sciences, Department of Medicine, University of Auckland, Auckland, New Zealand
  2. 2Department of Surgery, North Shore Hospital, Waitemata District Health Board, Auckland, New Zealand
  3. 3Department of Endocrinology, North Shore Hospital, Waitemata District Health Board, Auckland, New Zealand
  4. 4Faculty of Medical and Health Sciences, Department of Surgery, University of Auckland, Auckland, New Zealand
  1. Correspondence to Dr Rinki Murphy; R.Murphy{at}auckland.ac.nz

Abstract

Introduction Type 2 diabetes (T2D) in association with obesity is an increasing disease burden. Bariatric surgery is the only effective therapy for achieving remission of T2D among those with morbid obesity. It is unclear which of the two most commonly performed types of bariatric surgery, laparoscopic sleeve gastrectomy (LSG) and laparoscopic Roux-en-Y gastric bypass (LRYGB), is most effective for obese patients with T2D. The primary objective of this study is to determine whether LSG or LRYGB is more effective in achieving HbA1c<6% (<42 mmol/mol) without the use of diabetes medication at 5 years.

Methods and analysis Single-centre, double-blind (assessor and patient), parallel, randomised clinical trial (RCT) conducted in New Zealand, targeting 106 patients. Eligibility criteria include age 20–55 years, T2D of at least 6 months duration and body mass index 35–65 kg/m2 for at least 5 years. Randomisation 1:1 to LSG or LRYGB, used random number codes disclosed to the operating surgeon after induction of anaesthesia. A standard medication adjustment schedule will be used during postoperative metabolic assessments. Secondary outcomes include proportions achieving HbA1c<5.7% (39 mmol/mol) or HbA1c<6.5% (48 mmol/mol) without the use of diabetes medication, comparative weight loss, obesity-related comorbidity, operative complications, revision rate, mortality, quality of life, anxiety and depression scores. Exploratory outcomes include changes in satiety, gut hormone and gut microbiota to gain underlying mechanistic insights into T2D remission.

Ethics and dissemination Ethics approval was obtained from the New Zealand regional ethics committee (NZ93405) who also provided independent safety monitoring of the trial. Study commenced in September 2011. Recruitment completed in October 2014. Data collection is ongoing. Results will be reported in manuscripts submitted to peer-reviewed journals and in presentations at national and international meetings.

Trial registration numbers ACTRN12611000751976, NCT01486680; Pre-results.

  • type 2 diabetes
  • bariatric surgery
  • morbid obesity
  • Roux-en-Y gastric bypass
  • Sleeve gastrectomy

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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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