← Eichor
Study identifier: NCT05242835 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Management of Sleeve Gastrectomy Failure Using Single-anastomosis Metabolic Surgery

Condition: Obesity · Obesity, Morbid  ·  Sponsor: Laval University

PhaseNA
Planned participants151
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

Sleeve gastrectomy (SG) has become the most commonly performed weight loss surgery, accounting for 60% of all bariatric operations worldwide. While technically easier with less side-effects and nutritional risks than other operations, SG is also associated with a higher risk of failure (20 to 40%). In such case, the most effective option consists in adding an intestinal bypass called the Biliopancreatic Diversion with Duodenal Switch (BPD-DS). This surgery is, however, technically challenging and yields a significant risk of complications, nutritional deficiencies or gastro-intestinal side-effects. Recently, a simplified version of the Standard DS, called Single-Anastomosis Duodenoileal Switch (SADI-S) was endorsed by surgical societies as one of the approved bariatric procedures. There is currently no prospective or randomized data to support the effectiveness of this new procedure, especially as a revisional approach. The Overall Objective of this randomized controlled trial project is to establish the clinical benefits of the SADI-S as a revisional surgery after SG, while also considering critical issues related to sex and gender. The investigator Overall Hypothesis is that the SADI-S represents a relevant revisional option for weight loss and metabolic recovery in women and men suffering from severe obesity who had a previous SG. The investigator propose to address the following research question. Research Question: What are the clinical effects of SADI-S compared to sta…

This description comes directly from the study's public registry record.

Talk to the study team

Mélanie Nadeau, MSc  ·  418-656-8711  ·  melanie.nadeau@criucpq.ulaval.ca

Suzy Laroche  ·  418-656-8711  ·  suzy_laroche@ssss.gouv.qc.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Institut Universitaire de Cardiologie et de Pneumologie de QuébecQuébec, Quebec, CanadaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05242835