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Non-randomized Prospective Comparison Between SASI Bipartition and RYGB

NCT04469712 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 280

Last updated 2025-02-06

No results posted yet for this study

Summary

The main aim of this project is to assess the safety and efficiency of the SASI Bipartition.

Conditions

  • Obesity, Morbid
  • Metabolic Syndrome
  • Bariatric Surgery Candidate
  • Postoperative Complications

Interventions

PROCEDURE

SASI Bipartition

SASI Bipartition is performed with a sleeve gastrectomy over a 32 French gastric bougie and a 300 cm common limb. Side-to-side gastroileostomy with a diameter of approximately 2.5 cm at the anterior part of antrum, 6 cm proximal to pylorus.

PROCEDURE

Gastric bypass

A small gastric pouch (15 mL) is created, and the jejunum brought up as an antecolic and antegastric fashion. Routine limb lengths were 150 cm for the alimentary limb and 60 cm for the bilio-pancreatic limb. Both mesenteric defects are closed with the Endohernia® stapler.

Sponsors & Collaborators

  • Aleris Hospital

    lead OTHER

Principal Investigators

  • Ebrahim Aghajani, PhD · Aleris Hospital

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-01
Primary Completion
2027-07-01
Completion
2027-08-01

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04469712 on ClinicalTrials.gov