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NCT00002064 Clinical Trial

Toxoplasmic Encephalitis in Patients With AIDS. Treatment and Prevention of Relapse

HIV Infections Clinical Trial

Official title:
Toxoplasmic Encephalitis in Patients With AIDS. Treatment and Prevention of Relapse

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00002064
Other study ID # 021A
Secondary ID
Status Completed
Phase N/A
First received November 2, 1999
Last updated June 23, 2005

Study information
Verified date June 1989
Source NIH AIDS Clinical Trials Information Service
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

To compare pyrimethamine and intravenous (IV) clindamycin vs. pyrimethamine and sulfonamides in the treatment of AIDS patients with central nervous system (CNS) Toxoplasma gondii.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Exclusion Criteria

Co-existing Condition:

Patients with the following conditions are excluded:

- Opportunistic infection (Pneumocystis carinii pneumonia (PCP), cryptococcal meningitis) or other conditions (brain abscess) which would make treatment results difficult to interpret due to concurrent infection, disease, or therapy.

Patients with other opportunistic infections or brain diseases are excluded.

Patients with AIDS and cerebral toxoplasmosis.

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Pyrimethamine

• Clindamycin

Locations
Country Name City State
United States Palo Alto Med Foundation Palo Alto California

Sponsors (1)
Lead Sponsor Collaborator
Palo Alto Medical Foundation

Country where clinical trial is conducted

United States, 

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