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Trials / Completed

CompletedNCT03160261

Effect of Exenatide on Cortisol Secretion

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
10 (actual)
Sponsor
University of Tartu · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The primary aim of the study is to describe the effect of single dose of 10 micrograms (μg) exenatide given subcutaneously (s/c) on cortisol secretion. Secondary outcomes involve ACTH and glucose levels.

Detailed description

Exenatide is a short-acting Glucagon-Like Peptide receptor 1 (GLP-1 R) agonist. The clinical trial is conducted in10 healthy volunteers. Each subject receives one dose of subcutaneous exenatide (10 μg). After that, hormonal and physiological changes are measured during two hours. The blood samples are taken in 30-minute intervals. The primary endpoint is peak value of cortisol achieved during the 2 hours after drug administration.

Conditions

Interventions

TypeNameDescription
DRUGExenatide InjectionSingle injection of Exenatide 10μg subcutaneously

Timeline

Start date
2017-09-07
Primary completion
2017-12-28
Completion
2017-12-28
First posted
2017-05-19
Last updated
2018-05-03

Locations

1 site across 1 country: Estonia

Source: ClinicalTrials.gov record NCT03160261. Inclusion in this directory is not an endorsement.

Effect of Exenatide on Cortisol Secretion (NCT03160261) · Clinical Trials Directory