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A Study of Different Doses of Megestrol Acetate in Patients With AIDS Who Have Anorexia and Malnutrition

Primary Purpose

Anorexia, Cachexia, HIV Infections

Status
Completed
Phase
Phase 2
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 T-Lymphocytes, Megestrol, Dose-Response Relationship, Drug, Acquired Immunodeficiency Syndrome, Anorexia, Cachexia

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. 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

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
NCT00002300
Brief Title
A Study of Different Doses of Megestrol Acetate in Patients With AIDS Who Have Anorexia and Malnutrition
Official Title
Phase II-III Randomized Double-Blind Study Comparing Megestrol Acetate at 100, 400, and 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 characterize dose response in relation to weight gain. 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
T-Lymphocytes, Megestrol, Dose-Response Relationship, Drug, Acquired Immunodeficiency Syndrome, Anorexia, Cachexia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
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. 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.
Facility Information:
Facility Name
Birmingham Veterans Administration Med Ctr / Univ of Alabama
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Dr NS Tchekmedyian
City
Long Beach
State/Province
California
ZIP/Postal Code
90801
Country
United States
Facility Name
Dr Stephen J Gabin Jr
City
Los Angeles
State/Province
California
ZIP/Postal Code
90067
Country
United States
Facility Name
Eisenhower Med Ctr
City
Rancho Mirage
State/Province
California
ZIP/Postal Code
92270
Country
United States
Facility Name
Denver Public Health Dept
City
Denver
State/Province
Colorado
ZIP/Postal Code
80204
Country
United States
Facility Name
George Washington Univ Med Ctr
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20037
Country
United States
Facility Name
Veterans Administration Med Ctr
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20422
Country
United States
Facility Name
Miami Veterans Administration Med Ctr
City
Miami
State/Province
Florida
ZIP/Postal Code
33125
Country
United States
Facility Name
Northwestern Univ Med School
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Albany Med College / AIDS Treatment Ctr
City
Albany
State/Province
New York
ZIP/Postal Code
12203
Country
United States
Facility Name
Community Research Initiative on AIDS
City
New York
State/Province
New York
ZIP/Postal Code
10010
Country
United States
Facility Name
Saint Vincent's Hosp and Med Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10011
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
Univ of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Audie L Murphy Veterans Administration Hosp
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78284
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 of Different Doses of Megestrol Acetate in Patients With AIDS Who Have Anorexia and Malnutrition

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