LivingGLP1
Study S000912

Exenatide for Myocardial Protection During Reperfusion Study: A Double-blind, Placebo-controlled Trial

Registration

Registration
NCT01938235
Acronym
EMPRES
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
UNKNOWN
Enrollment
198
Start
2014-02
Primary completion
2017-07
Lead sponsor
University Health Network, Toronto
Conditions
Myocardial Infarction
Interventions
DRUG:Exenatide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED
Secondary identifiers
OTHER:9427-D0416-21C

Registered primary outcomes

  • Ratio of final infarct size at 3 months over area at risk at 72 hours post randomization (using cMRI) [3 months]

Linked records (0)

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