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Study identifier: NCT07565051 Synced from ClinicalTrials.gov · July 28, 2026
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Can Pre-operative Lean Mass Predict Weight Loss After Roux-en-Y Gastric Bypass?

Condition: Morbid Obesity Requiring Bariatric Surgery  ·  Sponsor: University Hospital, Geneva

PhaseN/A
Planned participants91
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The goal of this observational study is to evaluate whether preoperative fat-free mass predicts post-operative weight loss in patients undergoing Roux-En-Y gastric bypass. The primary objective of this study is to evaluate whether preoperative fat-free mass predicts weight loss in the two years following RYGB. The investigators will collect the following data, assessed as part of routine follow-up: * height, weight, hip and waist circumferences * body composition by bioimpedance analysis and dual energy-X-ray absorptiometry * Muscle strength and physical activity * Nutritional parameters: resting energy expenditure, eating behavior and digestive tolerance", plasma micronutrient status. . * Cardiovascular risk factors: fasting glucose, blood levels of Hb1Ac, triglycerides, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, blood pressure * Co-morbidities: joint pain and arthritis, sleep apnea, gastro-oesophageal reflux, metabolic dysfunction-associated fatty liver disease (MAFLD), cancer, stroke, heart attack. Quality of life: quality of life by the "Bariatric Analysis and Reporting Outcome (BAROS) questionnaire", symptoms of dumping syndrome by the "Sigstad diagnostic score system" Birthdate, birthweight and term of their children

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

Talk to the study team

Laurence Genton, MD  ·  0041 79 553 34 84  ·  laurence.genton@hug.ch

Laure Wilmart-Beck  ·  0041 22 372 93 49  ·  laure.wilmart@hug.ch

Always discuss trial participation with your own doctor first.

Locations (1)

Geneva University HospitalsGeneva, Canton of Geneva, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT07565051