LivingGLP1
Study S001322

EXEnatide in Patients Undergoing Coronary Artery Bypass Grafting for Improved glUcose conTrol and hemodynamIc ValuEs

Registration

Registration
NCT01373216
Acronym
Executive
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
SINGLE
Status
COMPLETED
Enrollment
38
Start
2011-06
Primary completion
2014-05
Lead sponsor
Charles University, Czech Republic
Conditions
Coronary Artery Disease; Decreased Left Ventricular Function
Interventions
DRUG:Exenatide
Results posted
FALSE

Registered primary outcomes

  • Cardiac function - echocardiographic parameters [90 days after administration of exenatide]

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
R0021691Effect of continuous exenatide infusion on cardiac function and peri-operative glucose control in patients undergoing cardiac surgery: A single-blind, randomized controlled trial.
Lipš M, Diabetes, obesity & metabolism
2017Randomized trialPMID 28581209DOIcites ClinicalTrials.gov:NCT01373216; registry reference DERIVED:28581209