A two-center randomized clinical superiority trial of single-anastomosis sleeve ileal bypass versus sleeve gastrectomy for severe obesity: SASSY study protocol.

Scand J SurgAug 5, 2026 (epub)

Helene M Haug, Rolf E Hagen, Jon A Kristinsson et al.

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In 30 seconds

The SASSY study is a two-center randomized clinical trial comparing single-anastomosis sleeve ileal bypass to sleeve gastrectomy in patients with class II and III obesity. The primary endpoint is the change in body mass index from baseline to 2 years post-surgery. This trial aims to provide robust data on the efficacy and safety of these surgical options.

Key findings

  • Primary endpoint: change in body mass index from baseline to 2 years post-surgery.
  • Secondary endpoints include weight loss outcomes, prevalence of gastroesophageal reflux disease, and quality of life.
  • Evaluations will occur at 2 and 5 years after surgery.

Why it matters

Understanding the comparative effectiveness and safety of single-anastomosis sleeve ileal bypass versus sleeve gastrectomy is crucial for optimizing treatment strategies in patients with severe obesity and related comorbidities.

Source

Published in Scand J Surg. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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