LivingGLP1
Study S000569

Prednisolone-induced Impairment of Glucose Metabolism and Beta-cell Dysfunction and the Protective Effects of Exenatide: a Single-center, Randomized, Double-blind, Placebo-controlled Crossover Study in Healthy Volunteers

Registration

Registration
NCT00744224
Acronym
PREDEX
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Status
COMPLETED
Enrollment
8
Start
2009-02
Primary completion
2010-01
Lead sponsor
Amsterdam UMC, location VUmc
Conditions
Glucocorticoid-induced Glucometabolic Abnormalities; Glucocorticoid-induced Beta-cell Dysfunction
Interventions
DRUG:Placebo; DRUG:Prednisolone; DRUG:Prednisolone and Exenatide
Results posted
FALSE

Registered primary outcomes

  • To assess whether a single day infusion of the GLP-1 RA exenatide, as compared to placebo, reverses GC-induced impairment of glucose metabolism in healthy males, quantified as glucose tolerance (AUCgluc) during a standardized mixed-meal test [Single-day treatment]

Linked records (1)

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
R0014060Glucagon-like peptide-1 receptor agonist treatment prevents glucocorticoid-induced glucose intolerance and islet-cell dysfunction in humans.
van Raalte DH, Diabetes care
2011Randomized trialPMID 21216851DOIcites ClinicalTrials.gov:NCT00744224; registry reference DERIVED:21216851