LivingGLP1
Study S001699

Exenatide-test for Diagnosing Endogenous Hyperinsulinemic Hypoglycemia

Registration

Registration
NCT04909333
Acronym
FAST
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Status
COMPLETED
Enrollment
29
Start
2021-04-29
Primary completion
2024-04-30
Lead sponsor
University Hospital, Basel, Switzerland
Conditions
Endogenous Hyperinsulinism
Interventions
DRUG:Exenatide; DRUG:0.9% saline solution
Results posted
FALSE

Registered primary outcomes

  • time to symptomatic hypoglycemia after exenatide test compared to placebo [within 4 hours after injection]

Linked records (2)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0011293Exenatide for diagnosing endogenous hyperinsulinemic hypoglycemia: a randomized placebo-controlled, double-blind, cross-over proof-of-principle study.
Hepprich M, European journal of endocrinology
2025Randomized trialPMID 40747712DOIcites ClinicalTrials.gov:NCT04909333; registry reference DERIVED:40747712
R0043934SAT-064 Copeptin Levels at Baseline and in Response to Short-Acting GLP-1 Receptor Agonists in Patients with Endogenous Hyperinsulinemic Hypoglycemia and Healthy Controls - A Secondary Analysis
Svenja Leibnitz, Journal of the Endocrine Society
2025Randomized trialDOIcites ClinicalTrials.gov:NCT04909333