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Depot Disulfiram for AIDS and ARC
This study has been completed.
Study NCT00002065   Information provided by NIH AIDS Clinical Trials Information Service
First Received: November 2, 1999   Last Updated: June 23, 2005   History of Changes

November 2, 1999
June 23, 2005
 
 
 
 
Complete list of historical versions of study NCT00002065 on ClinicalTrials.gov Archive Site
 
 
 
Depot Disulfiram for AIDS and ARC
Depot Disulfiram for AIDS and ARC

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

 
 
Interventional
Treatment, Open Label
HIV Infections
Drug: Disulfiram
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
 
 
 

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.

Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00002065
 
024A
St. Vincent's Medical Center
 
 
NIH AIDS Clinical Trials Information Service
November 1999

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP