A Study of Different Doses of Megestrol Acetate in Patients With AIDS Who Have Anorexia and Malnutrition
Anorexia, Cachexia, HIV Infections
About this trial
This is an interventional treatment trial for Anorexia focused on measuring T-Lymphocytes, Megestrol, Dose-Response Relationship, Drug, Acquired Immunodeficiency Syndrome, Anorexia, Cachexia
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. Prior Medication: Allowed: Ganciclovir. Exclusion Criteria Co-existing Condition: Patients with the following are excluded: Dementia or evidence of mental incompetence which would preclude compliance with the protocol. 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. Concurrent Medication: Excluded: 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 eight weeks. (Patients may have been previously treated with AZT and failed or may currently be receiving AZT for at least 8 weeks.) Patients with the following are excluded: Obstruction to food intake or impaired digestive/absorptive functions. Contraindications to high-dose 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. 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. Clinical or radiologic evidence of ascites or pleural effusions. 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 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.) History of substance abuse and questionable current and future abstinence.
Sites / Locations
- Birmingham Veterans Administration Med Ctr / Univ of Alabama
- Dr NS Tchekmedyian
- Dr Stephen J Gabin Jr
- Eisenhower Med Ctr
- Denver Public Health Dept
- George Washington Univ Med Ctr
- Veterans Administration Med Ctr
- Miami Veterans Administration Med Ctr
- Northwestern Univ Med School
- Albany Med College / AIDS Treatment Ctr
- Community Research Initiative on AIDS
- Saint Vincent's Hosp and Med Ctr
- Mem Sloan - Kettering Cancer Ctr
- Univ of Pennsylvania
- Audie L Murphy Veterans Administration Hosp