LivingGLP1
Study S001132

Exenatide and Postprandial Endothelial Dysfunction: Effects and Mechanisms

Registration

Registration
NCT01181986
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE4
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
76
Start
2010-08
Primary completion
2012-12
Lead sponsor
Carl T. Hayden VA Medical Center
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:Exenatide SC; DRUG:Exenatide IV; DRUG:Placebo SC; DRUG:Exendin-9; DRUG:Placebo IV
Results posted
TRUE

Registered primary outcomes

  • Reactive Hyperemia Index (RHI) [0, 2, 4, 6 and 8 hours on Day 11 (Sub-study 1); 0 and 120 minutes on test Days 1, 2 & 3 (Sub-study 2)]

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