Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07350512

Investigating the Acute Effects of Increasing Alanine Exposure in Healthy Participants

Investigating the Effect of Glucagon on Cognitive Function and Cerebral Glucose Metabolism in Humans: A Pilot Study

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
15 (estimated)
Sponsor
Nicolai Jacob Wewer Albrechtsen · Academic / Other
Sex
All
Age
25 Years – 70 Years
Healthy volunteers
Accepted

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.

Detailed description

Two peripheral catheters will be placed in the antecubital vein of each arm for infusion of L-alanine and blood sampling respectively. The infusion rate of alanine will start at 1.4 μmol/kg/min and increase every 30 minutes over a 3-hour period, up to a maximum of 28 μmol/kg/min. The study day will last approximately 4 hours, and a maximal blood volume of 130 ml will be collected. Blood samples for the analysis of plasma glucagon, glucose, insulin, C-peptide etc. will be drawn every 15 minutes.

Conditions

Interventions

TypeNameDescription
OTHERalanineA three-hour intravenous infusion with alanine with increasing infusion rate (from 1.4 μmol/kg/min and to 28 μmol/kg/min)

Timeline

Start date
2026-01-20
Primary completion
2026-09-30
Completion
2027-01-20
First posted
2026-01-20
Last updated
2026-01-20

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT07350512. Inclusion in this directory is not an endorsement.