A Study Comparing Megestrol Acetate at 800 mg/Day, and Placebo in AIDS Patients With Anorexia and Cachexia
Anorexia, Cachexia, HIV Infections
About this trial
This is an interventional treatment trial for Anorexia focused on measuring Body Weight, T-Lymphocytes, Nutritional Status, Megestrol, Acquired Immunodeficiency Syndrome, Anorexia, Cachexia, Energy Intake
Eligibility Criteria
Inclusion Criteria Patient must have: Confirmed diagnosis of AIDS (CDC definition). Documented weight loss or anorexia. Life expectancy = or > 20 weeks. The perception that the weight loss is a detriment to their well-being. Ability to provide informed consent, read and write English. Exclusion Criteria Co-existing Condition: Patients with the following conditions are excluded: Dementia or evidence of mental incompetence which would preclude compliance with the protocol. Severe diarrhea defined as 5 or more watery stools per day for at least 7 days. Active uncontrolled systemic infections at the start of treatment. Patients may not be entered for at least 2 weeks after acute infection. Clinical or radiologic evidence of ascites or pleural effusions. Patients with the following are excluded: Obstruction to food intake or impaired digestive/absorptive functions. Contraindications to megestrol acetate (poorly controlled hypertension or heart failure or deep vein thrombosis). Inability to consent or be available for close follow-up. Active systemic infections at the start of treatment. Clinical or radiologic evidence of ascites or pleural effusions. Patients who have been hospitalized or have suffered an exacerbation of their illness associated with weight loss within the past 2 weeks are excluded. Menstruating female patients are excluded. Prior Medication: Excluded: Corticosteroids. Anabolic steroids. Marijuana. Megestrol acetate. Patients who have been started on zidovudine (AZT) within 8 weeks. (Patients may have been previously treated with AZT and failed or may currently be receiving AZT for at least 8 weeks.) Patients may not be started on any therapy designed to treat the underlying HIV infection or which may have a major impact on appetite and/or weight gain. Patients who have been started on zidovudine (AZT) within 8 weeks. (Patients may have been previously treated with AZT and failed or may currently be receiving AZT for at least 8 weeks.) History of substance abuse and questionable current and future abstinence.
Sites / Locations
- Dr Mark Goldstein
- Summitt Med Ctr / San Francisco Gen Hosp
- Palo Alto Veterans Adm Med Ctr / Stanford Univ
- Eisenhower Med Ctr
- UCD Med Ctr
- San Francisco AIDS Clinic / San Francisco Gen Hosp
- San Francisco Veterans Administration Med Ctr
- Denver Public Health Dept
- Miami Veterans Administration Med Ctr
- Univ of South Florida
- Northwestern Univ Med School
- Mem Sloan - Kettering Cancer Ctr
- SUNY / Health Sciences Ctr at Syracuse
- Northwest Family Ctr at the Harbor View Med Ctr