Sleeve Gastrectomy Clinical Trials

Clinical trials related to Sleeve Gastrectomy Procedure

A Prospective Randomized Controlled Trial Comparing Revisional Laparoscopic Roux-en-Y Gastric Bypass Versus Ringed Revisional Roux-en-Y Gastric Bypass After Laparoscopic Sleeve Gastrectomy: 5-Year Outcomes on Weight Loss, BAROS Score, Quality of Life, and Food Tolerance

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Obesity remains a major global health challenge, with rising prevalence and significant metabolic, cardiovascular, and gastrointestinal comorbidities. Laparoscopic sleeve gastrectomy (LSG) has emerged as the most widely performed bariatric procedure due to its technical simplicity and satisfactory short- to mid-term results. However, a proportion of patients experience suboptimal weight loss, recurrent weight gain, or both. In this study, patients with recurrent weight gain of maximum weight loss or suboptimal weight loss or both following sleeve gastrectomy were included. Suboptimal weight loss is defined as total weight loss (TWL) of less than 20% of the preoperative weight and/or excess weight loss (EWL) of less than 50%, measured at least 12-18 months after the primary sleeve gastrectomy. Recurrent weight gain after sleeve gastrectomy is defined as an increase of ≥20% of the maximum weight loss (from nadir weight) or an increase in BMI of \>5, measured at least 24 months after the primary procedure.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Adults aged 18-65 years.

• Patients who experienced recurrent weight gain, suboptimal weight loss, or both within 12-24 months or more following sleeve gastrectomy.

• Eligible and fit for bariatric surgery.

• Willing to provide informed consent and adhere to follow-up.

Locations
Other Locations
Egypt
The surgical department of Medical Research Institute Hospital, Alexandria University
RECRUITING
Alexandria
Contact Information
Primary
Mohamed H Ashour, PhD
dr.mhany@gmail.com
00201002600970
Time Frame
Start Date: 2026-03-15
Estimated Completion Date: 2031-03
Participants
Target number of participants: 240
Treatments
Active_comparator: Group non banded
Standard revisional RYGB
Active_comparator: Group banded
Revisional Banded RYGB
Sponsors
Leads: General Committee of Teaching Hospitals and Institutes, Egypt

This content was sourced from clinicaltrials.gov