Clinical Trial

Investigating the Acute Effects of Increasing Alanine Exposure in Healthy Participants

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Summary
In this study the investigators will investigate the acute effects of increasing alanine exposure on metabolic parameters in healthy participants. Participants will participate in one study day. After initial baseline blood samples, a three-hour intravenous infusion with glucagon will be initiated. The infusion rate will be increased every 30 minutes.
Trial Details
NCT Number NCT07350512
Lead Sponsor Nicolai Jacob Wewer Albrechtsen
Conditions Glucose Metabolism, Glucagon
Enrollment 15 participants
Start Date 2026-01-20
Primary Completion 2026-09-30 (estimated)
Study Completion 2027-01-20 (estimated)
Updated on ClinicalTrials.gov 2026-01-20