Morbid Obesity Clinical Trial
Official title:
Bariatric Surgery Plus Weight Watchers vs. Weight Watchers in Underserved Minorities: Randomized Controlled Cross-over Trial
NCT number | NCT01929850 |
Other study ID # | 12-10409 |
Secondary ID | |
Status | Withdrawn |
Phase | Phase 4 |
First received | August 15, 2013 |
Last updated | May 6, 2015 |
Obesity is a costly multi-etiology world disease of fat storage. Morbid obesity is defines as greater than 100 pounds overweight and/or greater than 200 % of ideal body weight. Chronic underemployment, poor housing, child abuse, limited education, stress and anxiety are all associated with maternal morbid obesity. These latter conditions leave many patients in a state of economic, social and emotional poverty with need for life-long welfare support. For patients with true morbid obesity a standard surgical procedure is currently the procedure of choice especially among patients who fail standard medical intervention. The major procedures performed for morbid obesity include the Roux-en-Y gastric bypass, sleeve gastrectomy and laparoscopic band procedure. The sleeve gastrectomy is purely a restrictive procedure without malabsorptive components which involves one single staple line and can be performed laparoscopically in less than one hour. While these surgical procedures are recognized as "standard" procedures for patient who have failed medical treatment and are "covered" by most health plans, access to these procedures is limited for the medically underserved, rural, poor or underrepresented minorities since national, state and municipal health plans either provide minimal coverage or no coverage at all for surgery for morbid obesity. Reimbursement to providers offering these procedures is minimal and thus access to bariatric surgery is unlikely within a timely fashion.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | October 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: Patients who are morbidly obese. 1. Female, age 18-65 years 2. Meeting the criteria as outlined in Part 2 A (Synopsis) of a medically underserved, rural, poor or underrepresented minority. 3. BMI > 40 and < 55, or BMI > 35 and <55 with one or more significant comorbidities. Co-morbidities are defined as diabetes, pulmonary disease, cardiac disease, or hypertension [systolic blood pressure of =140 mm Hg or diastolic blood pressure =90 mm Hg (or both) or on treatment for hypertension] 4. History of obesity for at least 2.5 years 5. History of failure with non-surgical weight loss methods 6. Agree to comply with the substantial dietary restrictions and exercise program required by the procedure 7. Signed approval by physician and psychologist of subject's physical and mental suitability for bariatric surgery 8. Understands risks of procedures, agree to follow protocol requirements, including signing informed consent, returning for follow-up visits and completing all required testing, completing diet and behavior modification counseling. 9. Subject is a resident within the state of California or the city of Bangkok, Thailand and will likely remain so for a 2 year period of time. 10. Willingness to participate in weekly visits with Weight Watchers International local program. Exclusion Criteria: 1. Subject history of inflammatory disease of the gastrointestinal tract including Crohn's disease or ulcerative colitis 2. Significant known esophageal disease including grade 3-4 esophagitis, active gastric ulcer disease or active duodenal ulcer disease 3. Severe coagulopathy, upper GI bleeding conditions such as esophageal or gastric varices, congenital or acquired telangiectasia 4. Congenital or acquired anomalies of the GI tract such as atresias or stenoses. 5. Severe cardiopulmonary disease or other serious organic disease including HIV or cancer 6. Currently pregnant or nursing. Potentially childbearing (i.e. not post-menopausal or surgically sterilized) and not willing to use an effective method of contraception for the next 12 months 7. Current alcohol or drug addiction 8. Mentally retarded or emotionally unstable, or exhibits psychological characteristics which, in the opinion of the investigator or psychologist/psychiatrist, make the subject a poor candidate for this procedure 9. Previous gastric, esophageal, pancreatic, or bariatric surgery 10. Infection anywhere in the body at the time of the procedure 11. Subject history of scleroderma, amyloidosis 12. Thyroid disease which is not controlled with medication 13. Hormonal or genetic cause for the obese state. 14. History of cancer other than localized basal cell carcinoma. 15. Myocardial infarction or cerebrovascular accident within past year. 16. Angina pectoris. 17. Severe coagulopathy (prothrombin time > 3 seconds over control or platelet count < 100,000) 18. Gastroparesis or pyloric stenosis. 19. Lesions with increased risk of bleeding. 20. Severe cardiopulmonary disease or other serious organic disease, including HIV or cancer. 21. Congestive heart failure. 22. Uncontrolled hypertension (systolic > 150 or diastolic > 100). 23. Severe or advanced liver disease (such as cirrhosis, chronic hepatitis, portal hypertension, etc.). 24. Severe reflux disease. 25. Active, continuous alcohol consumption (> 80 gm/day of ethanol) or chronic illicit drug use within the last 3 years. 26. Currently on prescription or over the counter diet drugs. 27. Chronic therapy with aspirin, NSAID or anticoagulants. 28. Not ambulatory. 29. Participating in another ongoing clinical trial in which concomitant diagnosis or therapeutic intervention would adversely affect the integrity of the clinical trial. |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | UCSF/San Francisco General Hospital | San Francisco | California |
Lead Sponsor | Collaborator |
---|---|
University of California, San Francisco |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | body mass index (BMI) | Comparison of body mass index (BMI) in underserved young women treated with laparoscopic sleeve gastrectomy plus Weight Watchers vs. Weight Watchers alone for the treatment of morbid obesity . | One year post randomization (% of patients with reduction in BMI by 5 points) | Yes |
Secondary | quality of life | Determine the effect of treatment on quality of life, employability, income levels, overall costs to society and co-morbidities | One year after study completion | No |
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