LivingGLP1
Study S000487

A Pilot Study Evaluating Exenatide for the Treatment of Postprandial Hyperinsulinemic Hypoglycemia Post-RYGB

Registration

Registration
NCT02685852
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
11
Start
2016-02
Primary completion
2019-07-22
Lead sponsor
University of Minnesota
Conditions
Hyperinsulinemic Hypoglycemia
Interventions
DRUG:Exenatide; DRUG:Acarbose; DRUG:Exenatide Placebo; DRUG:Acarbose Placebo
Results posted
FALSE

Registered primary outcomes

  • Glucose area under the curve (AUC) following treatment for each 4-hour test period [During the 4-hour test period]
  • Presence of hypoglycemia [15, 30, 45, 60, 90, 120, 180 and 240 minutes]

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