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COMPLETED
NCT02860923
PHASE3

Efficacy and Safety of Exenatide in the Treatment of Hypothalamic Obesity After Craniopharyngioma Therapy

Sponsor: University Hospital, Bordeaux

View on ClinicalTrials.gov

Summary

This hypothalamic obesity is associated with serious metabolic and psychosocial consequences. The purpose of the study is to compare the change of body weight after 6 months treatment with a lifestyle intervention + exenatide compare to the one after the same lifestyle intervention+ placebo in adults patients suffering from a hypothalamic obesity due to treatment of craniopharyngioma.

Official title: Multicentre Double-blind Randomized Clinical Trial Assessing Efficacy and Safety of Exenatide in the Treatment of Hypothalamic Obesity After Craniopharyngioma Therapy

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

42

Start Date

2017-01-11

Completion Date

2018-09-30

Last Updated

2026-05-22

Healthy Volunteers

No

Interventions

DRUG

Exenatide

DRUG

Placebo

Locations (11)

CHU d'Angers

Angers, France

CHU de Brest

Brest, France

CHU de Grenoble

Grenoble, France

CHU de Lyon

Lyon, France

APHM

Marseille, France

Hôpital Bicêtre

Paris, France

Hôpital Cochin

Paris, France

Hôpital Européen Georges Pompidou

Paris, France

Hôpital Pitié Salpétrière (APHP)

Paris, France

Hôpital Haut-Lévêque

Pessac, France

CHU de Toulouse

Toulouse, France