Expired Study
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Honolulu, Hawaii 96813


Purpose:

To evaluate the efficacy of dinitrochlorobenzene (DNCB) in patients with early HIV infection by monitoring immunologic parameters and serum HIV RNA. To facilitate the understanding of possible alterations in the immunological status of the HIV+ patient cohort.


Criteria:

Inclusion Criteria Patients must have: - EITHER HIV negative or documented HIV+ by both the ELISA and Western blot tests. For HIV+ patients: - Patients must fail to meet the AIDS-defining criteria. - CD4 lymphocyte count between 200 - 500 cells/mm3. Exclusion Criteria Co-existing Condition: Excluded: Patients with obvious ultra violet(UV)-irradiated skin damage in the treatment sites. Concurrent Medication: Excluded: - Patients who are likely to commence antiretrovirals within the 6-month study period. - Patients using other immunomodulator therapies or other alternative therapies. - Patients likely to require chemotherapy during the course of the study. Concurrent Treatment: Excluded: - Patients who are likely to require significant UV light exposure during the study period. - Patients who are likely to require radiation therapy during the course of the study. Prior Medication: Excluded: - Prior exposure to DNCB. - Patients who have used antiretroviral medications within the previous 3 months.


NCT ID:

NCT00002175


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Honolulu, Hawaii 96813
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: September 21, 2017

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