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Clinical Trial Summary

The goal of this study is to understand how exogenous kisspeptin affects metabolism by evaluating responses to an oral glucose tolerance test


Clinical Trial Description

Assignment: Each study subject will serve as their own control. The order of the visits will be randomized. Delivery of Interventions: - Prior to the study visit, subjects will undergo a review of their medical history and screening laboratories. - During the inpatient study, the subjects will - Undergo a 16-hour kisspeptin infusion - Undergo an oral glucose tolerance test ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04958109
Study type Interventional
Source Massachusetts General Hospital
Contact Margaret Lippincott, MD
Phone 617-726-8434
Email MGHKisspeptinResearch@partners.org
Status Recruiting
Phase Phase 1
Start date October 28, 2021
Completion date August 2024

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