Clinical Trial

Glucagon Dose-Response in Patients With Post-Bariatric Hypoglycemia

Active, Not Recruiting Phase 4
View on ClinicalTrials.gov →
Record status
This record was last updated February 6, 2026 (before its estimated June 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
The purpose of the study is to determine how blood sugar levels in individuals with and without hypoglycemia after bariatric surgery respond to different doses of glucagon, a hormone that is usually present in your body that regulates blood sugar levels. In this study, there will be 4 visits to the clinical research center. In the first visit, medical history and physical exam will be performed, and blood samples will be taken to assess overall health. During visit 2, a continuous glucose monitor will be placed under the skin. (This may be combined with visit 1, depending on the schedule of visits.) In visit 3, we will test the effect of a total of 4 different doses of glucagon, in increasing doses. In visit 4, we will test the effect of a total of 3 doses of glucagon, in decreasing doses. For both visit 3 and 4, we will infuse labeled stable glucose to allow us to measure how much glucose the body is making, and will measure levels of hormones which regulate glucose, such as insulin and glucagon.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-05-15; most recent amendment 2026-02-04.
Status change: Recruiting → Active, Not Recruiting 2026-02-04
Trial Details
NCT Number NCT06986603
Lead Sponsor Joslin Diabetes Center
Collaborators: University of Alabama at Birmingham, University of Virginia, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Conditions Hypoglycemia, Hypoglycemia, Reactive, Bariatric Surgery
Enrollment 28 participants
Start Date 2024-11-26
Primary Completion 2026-06-01 (estimated)
Study Completion 2026-09-01 (estimated)
Updated on ClinicalTrials.gov 2026-02-06