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A Study Comparing Megestrol Acetate at 800 mg/Day, and Placebo in AIDS Patients With Anorexia and Cachexia

Primary Purpose

Anorexia, Cachexia, HIV Infections

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Megestrol acetate
Sponsored by
Bristol-Myers Squibb
About
Eligibility
Locations
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
October 1, 2007
Sponsor
Bristol-Myers Squibb
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1. Study Identification

Unique Protocol Identification Number
NCT00002067
Brief Title
A Study Comparing Megestrol Acetate at 800 mg/Day, and Placebo in AIDS Patients With Anorexia and Cachexia
Official Title
Phase III Randomized Double-Blind Study Comparing Megestrol Acetate at 800 mg/Day, and Placebo in AIDS Patients With Anorexia and Cachexia
Study Type
Interventional

2. Study Status

Record Verification Date
October 2007
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Bristol-Myers Squibb

4. Oversight

5. Study Description

Brief Summary
To compare the effects of megestrol acetate and placebo on body weight, anorexia, cachexia, calorie intake, and nutritional parameters of patients with a confirmed diagnosis of AIDS. To determine whether megestrol acetate relative to placebo improves the perception of well-being among AIDS patients with cachexia. To evaluate megestrol acetate's effect on immune function via skin test reactivity, T4/T8 ratio, and total lymphocytes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anorexia, Cachexia, HIV Infections
Keywords
Body Weight, T-Lymphocytes, Nutritional Status, Megestrol, Acquired Immunodeficiency Syndrome, Anorexia, Cachexia, Energy Intake

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Masking
Double

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Megestrol acetate

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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.
Facility Information:
Facility Name
Dr Mark Goldstein
City
Los Angeles
State/Province
California
ZIP/Postal Code
90048
Country
United States
Facility Name
Summitt Med Ctr / San Francisco Gen Hosp
City
Oakland
State/Province
California
ZIP/Postal Code
94609
Country
United States
Facility Name
Palo Alto Veterans Adm Med Ctr / Stanford Univ
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304
Country
United States
Facility Name
Eisenhower Med Ctr
City
Rancho Mirage
State/Province
California
ZIP/Postal Code
92270
Country
United States
Facility Name
UCD Med Ctr
City
Sacramento
State/Province
California
ZIP/Postal Code
95817
Country
United States
Facility Name
San Francisco AIDS Clinic / San Francisco Gen Hosp
City
San Francisco
State/Province
California
ZIP/Postal Code
941102859
Country
United States
Facility Name
San Francisco Veterans Administration Med Ctr
City
San Francisco
State/Province
California
ZIP/Postal Code
94121
Country
United States
Facility Name
Denver Public Health Dept
City
Denver
State/Province
Colorado
ZIP/Postal Code
80204
Country
United States
Facility Name
Miami Veterans Administration Med Ctr
City
Miami
State/Province
Florida
ZIP/Postal Code
33125
Country
United States
Facility Name
Univ of South Florida
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Facility Name
Northwestern Univ Med School
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Mem Sloan - Kettering Cancer Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
SUNY / Health Sciences Ctr at Syracuse
City
Syracuse
State/Province
New York
ZIP/Postal Code
13210
Country
United States
Facility Name
Northwest Family Ctr at the Harbor View Med Ctr
City
Seattle
State/Province
Washington
ZIP/Postal Code
98104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
9066597
Citation
Strang P. The effect of megestrol acetate on anorexia, weight loss and cachexia in cancer and AIDS patients (review). Anticancer Res. 1997 Jan-Feb;17(1B):657-62.
Results Reference
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A Study Comparing Megestrol Acetate at 800 mg/Day, and Placebo in AIDS Patients With Anorexia and Cachexia

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