Studies of Biological Changes Related to Weight Loss After Gastric Bypass Surgery
NCT ID: NCT00120562
Last Updated: 2009-08-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
13 participants
OBSERVATIONAL
2007-07-31
Brief Summary
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Detailed Description
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The initial assessment will be performed before the surgery (testing period 1). After surgery is completed, subjects will attend clinic visits at the Rockefeller University outpatient clinic. During these visits, weight and leptin levels will be monitored. Two additional assessments will be performed during weight loss, when subjects lose 10% and 20% of their initial weight (testing periods 2 and 3 respectively). A final evaluation will be performed after weight is stabilized, about 18 months after the surgery is completed (testing period 4). Each testing period will be performed over a 2 week period in an inpatient setting at the Rockefeller University Hospital. During testing periods subjects will undergo a series of metabolic, behavioral, hormonal, immune and molecular tests to evaluate changes that occur in the body after weight loss. Subjects will receive monetary compensation for participating in the study.
Conditions
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Keywords
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Study Design
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PROSPECTIVE
Interventions
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Gastric Bypass Surgery
Eligibility Criteria
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Inclusion Criteria
* Subjects approved for gastric bypass surgery
Exclusion Criteria
18 Years
65 Years
ALL
No
Sponsors
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New York Obesity and Nutrition Research Center
OTHER
Rockefeller University
OTHER
Principal Investigators
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Jeffrey M. Friedman, MD
Role: PRINCIPAL_INVESTIGATOR
Rockefeller University
Locations
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St. Luke's Obesity Research Center, NY NY 10023 and New York Hospital
New York, New York, United States
Countries
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Related Links
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Related Info
Other Identifiers
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JFN 0385
Identifier Type: -
Identifier Source: org_study_id