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Depot Disulfiram for AIDS and ARC

Depot Disulfiram for AIDS and ARC

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002065
Enrollment
Unknown
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2005-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Keywords

Delayed-Action Preparations, Disulfiram, Acquired Immunodeficiency Syndrome, AIDS-Related Complex

Brief summary

To assess the safety and efficacy of depot disulfiram as a new treatment for AIDS and AIDS related complex.

Interventions

DRUGDisulfiram

Sponsors

St. Vincent's Medical Center
Lead SponsorUNKNOWN

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients must have a positive diagnosis of AIDS or AIDS related complex (ARC) according to the CDC criteria. * Also patient must be: * Able to understand the study. * Strongly motivated to participate in the study, and willing to comply with all the conditions specified in the informed consent forms. * Ambulatory and able to maintain an independent life outside the hospital. * Free of clinically significant organic disease affecting neurologic, hepatic, renal, and clinical status. Patients must be free of clinically significant organic disease affecting neurologic, hepatic, renal, and clinical status. Patients must be free of clinically significant organic disease affecting neurologic, hepatic, renal, and clinical status. History of alcohol abuse.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026