Bioenergetic Alterations After Exenatide Administration

Completed · Phase 4

Conditions studied: Healthy

In brief

The purpose of this study is to find out how exenatide causes weight loss. Specifically, the study is assessing how exenatide may change how people take in energy (energy intake), as well as how it may effect how people use energy (energy expenditure).

Key facts

Study ID

NCT00623545

Run by

University of Wisconsin, Madison

People needed

28

Starts

2008-01-01

Expected to finish

2010-04-01

Last updated by the study team

2015-01-09

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 18-65 years of age
• BMI between 30 and 40 kg/m2
• Women with a negative pregnancy test at baseline, who are sterile, using contraceptives or in a committed relationship with someone who is sterile or using contraception
• Absence of weight change greater than 3 kg in the previous 6 months

You may not qualify if…

• Women who are pregnant or lactating
• Current or recent (6 months) enrollment in a commercial or self prescribed weight loss or exercise program
• Use of weight loss medication
• A history of metabolic disease i.e. renal, endocrine, hepatic or gastrointestinal disease that would impact the outcome of the study
• Presence of medical conditions that are known to affect energy expenditure (i.e. hyperthyroidism, rheumatoid arthritis, AIDS among others)
• History of hypoglycemia
• A history of psychiatric or eating disorder
• Abnormal EKG
• Previous history of pancreatitis
• Previous history of gastroparesis or GI motility disorder
• Use of medications that can affect GI motility
• History of organ transplantation
• Other comorbid conditions which may preclude the subject's ability to complete the study
• Use of a carbonic anhydrase inhibitor such as acetazolamide

Where it is running

• Univ Wisconsin Hospital and Clinics — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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