A Randomized Controlled Prophylactic Study of Clofazimine To Prevent Mycobacterium Avium Complex Infection in HIV Disease
NCT ID: NCT00002058
Last Updated: 2005-06-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
INTERVENTIONAL
Brief Summary
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Detailed Description
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Conditions
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Study Design
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TREATMENT
Interventions
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Clofazimine
Eligibility Criteria
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Inclusion Criteria
Allowed:
* Pneumocystis prophylaxis.
* Antiretroviral therapy, or other experimental protocols.
* Antipyretics and analgesics as per the treating physician.
Exclusion Criteria
Patients with the following are excluded:
* Unexplained fever.
* Night sweats.
* Unexplained anemia with hemoglobin \< 10 g percent or hematocrit less than 30 percent.
* Hepatic transaminase elevations or total bilirubin values of \> 3 times normal.
* Long-term (over 2 weeks) treatment with any drug with known significant anti-Mycobacterium avium complex (MAC) activity including isoniazid, ethambutol, rifampin, raffia, PAS, PZA, amikacin, streptomycin, ethionamide, viomycin, cycloserine, capreomycin, ciprofloxacin, imipenem, rifapentine, gentamicin, or penicillin.
Patients with the following are excluded:
* Known hypersensitivity to clofazimine.
* Mycobacterium avium complex (MAC) infection diagnosis at any site (except isolation from stool in asymptomatic patient).
* Any of the following symptoms at the time of study entry:
* Unexplained fever.
* Night sweats.
* Unexplained anemia with hemoglobin \< 10 percent or hematocrit less than 30 percent.
* Hepatic transaminase elevations or total bilirubin values of \> 3 times normal.
* Long-term (over 2 weeks) treatment with any drug with known significant anti-MAC activity.
Prior Medication:
Excluded:
* Long-term (over 2 weeks) treatment with any drug with known significant anti-Mycobacterium avium complex (MAC) activity including isoniazid, ethambutol, rifampin, raffia, PAS, PZA, amikacin, streptomycin, ethionamide, viomycin, cycloserine, capreomycin, ciprofloxacin, imipenem, rifapentine, gentamicin, or penicillin.
Group 1:
* AIDS patients with a first episode of Pneumocystis carinii pneumonia (PCP) within 2 to 4 months prior to study entry.
* Group 2:
* Patients with T4 counts \< 100 cells/mm3, regardless of prior opportunistic infections or malignancies.
* Karnofsky = or \> 70.
* All patients must sign informed consent.
18 Years
ALL
No
Sponsors
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University of California, San Francisco
OTHER
Locations
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Keith Med Group
Los Angeles, California, United States
San Francisco Gen Hosp
San Francisco, California, United States
Countries
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References
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Gustavson LE, Fukuda EK, Rubio FA, Dunton AW. A pilot study of the bioavailability and pharmacokinetics of 2',3'-dideoxycytidine in patients with AIDS or AIDS-related complex. J Acquir Immune Defic Syndr (1988). 1990;3(1):28-31.
Abrams DI, Mitchell TF, Child CC, Shiboski SC, Brosgart CL, Mass MM. Clofazimine as prophylaxis for disseminated Mycobacterium avium complex infection in AIDS. J Infect Dis. 1993 Jun;167(6):1459-63. doi: 10.1093/infdis/167.6.1459.
Other Identifiers
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027A
Identifier Type: -
Identifier Source: org_study_id