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NOT YET RECRUITING
NCT06287307
PHASE4

Semaglutide 2.4mg for Low Responders After Bariatric Surgery

Sponsor: Zuyderland Medisch Centrum

View on ClinicalTrials.gov

Summary

In 20 - 30% of the patients, the low responders, sufficient weight loss is not achieved after bariatric surgery. Secondary and/or tertiary bariatric procedures can lead to successful weight loss and resolution of comorbid conditions though, morbidity and mortality rates of these procedures are high. Therefore, additional pharmacotherapy has been suggested. Semaglutide is one of the medications that might improve outcome in the post-bariatric population. Semaglutide is a Glucagon-like peptide-1 (GLP-1) receptor analogue developed to treat type 2 diabetes. It causes glucose-dependent insulin secretion, promotes satiety and inhibits glucagon secretion. In obese (non-bariatric) patients, semaglutide has shown to improve glycemic control, decrease blood pressure, lower cardiovascular risk, and decrease body weight.

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

152

Start Date

2024-05

Completion Date

2026-09

Last Updated

2024-03-01

Healthy Volunteers

No

Interventions

OTHER

Placebo

The placebo will be used in the allocated group in addition to our lifestyle program for the duration of 68 weeks in total.

DRUG

Semaglutide 2.4 MG/0.75 ML Subcutaneous Solution [WEGOVY]

The semaglutide will be used in the allocated group in addition to our lifestyle program for the duration of 68 weeks in total.