LivingGLP1
Study S002161

Exenatide (Byetta) Vs Pramlintide (Symlin): Role in Post-prandial Hyperglycemia

Registration

Registration
NCT01269047
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE4
Masking
NONE
Status
COMPLETED
Enrollment
37
Start
2009-08
Primary completion
2016-08
Lead sponsor
Albert Einstein College of Medicine
Conditions
Type 1 Diabetes
Interventions
DRUG:Pramlintide; DRUG:Exenatide; DRUG:Insulin
Results posted
TRUE
Secondary identifiers
NIH:R01DK077166

Registered primary outcomes

  • Post-prandial Blood Glucose Concentration in Both Pramlintide and Exenatide Treated Groups in Acute and Chronic Setting, Compared to Insulin Monotherapy in Type 1 Diabetes Mellitus. [6 months]

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