LivingGLP1
Study S000826

A Pilot Study of the Effects of BYETTA® (Exenatide) on Weight Loss in Morbidly Obese Non Diabetic Patients Following Adjustable Gastric Banding

Registration

Registration
NCT00872378
Acronym
AGREE
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2; PHASE3
Masking
TRIPLE
Status
UNKNOWN
Enrollment
28
Start
2009-02
Primary completion
2010-12
Lead sponsor
Advanced Specialty Care
Conditions
Morbid Obesity
Interventions
DRUG:Exenatide; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • To describe change in body weight in non-diabetic morbidly obese patients after laparoscopic adjustable gastric banding (LAGB) with twice daily exenatide plus lifestyle modification plan or placebo plus lifestyle modification plan. [52 weeks]

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