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Clinical Trial Summary

The present study evaluates appetite, glucose metabolism, gastrointestinal motility and energy expenditure in men and women with obesity (BMI 30-40 kg/m2) under oxytocin exposure compared to placebo.


Clinical Trial Description

In a randomised, double-blind, placebo-controlled, crossover fashion, 24 participants will complete two experimental days (A and B) including a mixed meal test and an ad libitum meal test. The procedures during the two experimental days are similar except for intravenous infusion of oxytocin on experimental day A and placebo (saline) on experimental day B, respectively. On experimental days, oxytocin or placebo infusion will be started at timepoint -60 minutes. At timepoint 0 minutes, participants will ingest a liquid mixed meal. After 190 minutes, participants are served an ad libitum meal followed by ad libitum snacks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06189001
Study type Interventional
Source University Hospital, Gentofte, Copenhagen
Contact Ida Marie Gether, MD
Phone 004524246625
Email ida.marie.gether.01@regionh.dk
Status Recruiting
Phase N/A
Start date January 1, 2024
Completion date December 31, 2024

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