LivingGLP1
Study S002033

Intravenous Exenatide (Byetta®) Versus Insulin for Perioperative Glycemic Control in Cardiac Surgery: the Open-labeled Randomized Phase II/III ExStress Study

Registration

Registration
NCT01969149
Acronym
ExSTRESS
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2; PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
110
Start
2015-01
Primary completion
2015-12
Lead sponsor
Centre Hospitalier Universitaire de Besancon
Conditions
Stress Hyperglycemia
Interventions
DRUG:Exenatide; DRUG:Insulin
Results posted
FALSE

Registered primary outcomes

  • Percentage of patients spending more than 50 % of the time in the glycemic target range (100 to 140 mg/dl) [48 hours]

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
R0021932Impact of intravenous exenatide infusion for perioperative blood glucose control on myocardial ischemia-reperfusion injuries after coronary artery bypass graft surgery: sub study of the phase II/III ExSTRESS randomized trial.
Besch G, Cardiovascular diabetology
2018Randomized trialPMID 30384842DOIcites ClinicalTrials.gov:NCT01969149; registry reference DERIVED:30384842