A Study of Azidothymidine Plus Methadone in Patients With AIDS and AIDS Related Complex (ARC)

Sponsor
National Institute of Allergy and Infectious Diseases (NIAID) (NIH)
Overall Status
Completed
CT.gov ID
NCT00001008
Collaborator
(none)
18
1

Study Details

Study Description

Brief Summary

To determine if methadone treatment will affect the blood levels of zidovudine (AZT) in patients with AIDS or AIDS-related complex (ARC) who are receiving oral AZT and methadone therapy. In addition, the blood levels of methadone both before and during AZT treatment will be studied, and patients receiving daily oral methadone treatment will be evaluated for signs of narcotic withdrawal during treatment with AZT.

The number of deaths due to AIDS in high-risk populations continues to increase. Nationwide approximately 25 percent of AIDS patients are intravenous (IV) drug abusers, and it is very likely that an increasingly larger number of AIDS patients receiving AZT therapy will have had a history of IV drug abuse. The major chemical treatment for IV drug abuse is daily methadone maintenance therapy, and IV drug abusers who are HIV positive represent a large number of patients who will undergo long-term treatment with both methadone and AZT. Therefore, the study of potential drug interactions is essential.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

The number of deaths due to AIDS in high-risk populations continues to increase. Nationwide approximately 25 percent of AIDS patients are intravenous (IV) drug abusers, and it is very likely that an increasingly larger number of AIDS patients receiving AZT therapy will have had a history of IV drug abuse. The major chemical treatment for IV drug abuse is daily methadone maintenance therapy, and IV drug abusers who are HIV positive represent a large number of patients who will undergo long-term treatment with both methadone and AZT. Therefore, the study of potential drug interactions is essential.

The 18 patients are patients with AIDS or ARC. Nine are control patients who are not receiving methadone and are not IV drug abusers. Nine are former IV drug abusers who have been maintained on methadone for at least 6 months and who have been receiving a constant daily dose of methadone for at least 1 month. Plasma and urine levels of methadone are determined over a 4 hour period. The dose of AZT: For the pharmacokinetic study of AZT, plasma and urine samples are taken after oral dose of AZT and an intravenous dose of AZT in the control and methadone groups.

Study Design

Study Type:
Interventional
Intervention Model:
Parallel Assignment
Primary Purpose:
Treatment
Official Title:
Pharmacokinetic Study of the Interaction of Azidothymidine and Methadone in Patients With AIDS and ARC
Actual Primary Completion Date :
Mar 1, 1991

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Inclusion Criteria

    Prior Medication:
    Allowed:
    • Oral nonabsorbable antifungal agents.

    The study will include 18 patients with AIDS or HIV-related symptomatic illness as defined by the CDC classification group IVa and c2. Of these, 9 methadone recipients will have been maintained on methadone for at least 1 month and will have received a constant daily dose of 30-90 mg of methadone for at least 10 days.

    Nine patients will be former intravenous drug abusers.

    Exclusion Criteria

    Co-existing Condition:
    Patients with the following symptoms or conditions are excluded:
    • Temperature > 101 degrees F.

    • Ascites.

    • Active opportunistic infection.

    Concurrent Medication:
    Excluded:
    • Other inducers or inhibitors of hepatic microsomal enzymes.

    • Any chronic systemic medications.

    Patients with the following symptoms or conditions are excluded:
    • Temperature > 101 degrees F.

    • Ascites.

    • Active opportunistic infection.

    Prior Medication:
    Excluded within 72 hours of study entry:
    • All medication except oral nonabsorbable antifungal agents.

    • Excluded within 2 weeks of study entry:

    • Any other experimental drug.

    • Drugs with known nephrotoxic potential or drugs known to cause neutropenia.

    • Rifampin or its derivatives, phenytoin, or barbiturates.

    Active drug or alcohol abuse.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Montefiore Med Ctr / Bronx Municipal Hosp Bronx New York United States 10467

    Sponsors and Collaborators

    • National Institute of Allergy and Infectious Diseases (NIAID)

    Investigators

    • Study Chair: G Friedland,

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00001008
    Other Study ID Numbers:
    • ACTG 055
    First Posted:
    Aug 31, 2001
    Last Update Posted:
    Mar 14, 2011
    Last Verified:
    Aug 1, 1991

    Study Results

    No Results Posted as of Mar 14, 2011