Evaluation of the Epidermal Langerhans Cell Population in AIDS / ARC Patients by the Topical Application of a Potent Contact Allergen (1-Chloro-2,4-Dinitro-Chlorobenzene) (DNCB)
This study has been completed.
Sponsor:
University of California, San Francisco
Information provided by:
NIH AIDS Clinical Trials Information Service
ClinicalTrials.gov Identifier:
NCT00002031
First received: November 2, 1999
Last updated: June 23, 2005
Last verified: February 1990
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Purpose
To evaluate the effect of application of Dinitrochlorobenzene (DNCB) on the number, morphology, and antigen expression of epidermal Langerhans cells in AIDS and AIDS related complex (ARC) patients.
| Condition | Intervention |
|---|---|
|
HIV Infections |
Drug: Dinitrochlorobenzene |
| Study Type: | Interventional |
| Study Design: | Primary Purpose: Treatment |
| Official Title: | Evaluation of the Epidermal Langerhans Cell Population in AIDS / ARC Patients by the Topical Application of a Potent Contact Allergen (1-Chloro-2,4-Dinitro-Chlorobenzene) (DNCB) |
Resource links provided by NLM:
Genetics Home Reference related topics:
complement factor I deficiency
MedlinePlus related topics:
HIV/AIDS
U.S. FDA Resources
Further study details as provided by NIH AIDS Clinical Trials Information Service:
Eligibility| Ages Eligible for Study: | 18 Years to 55 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria
Patients must have the following:
- Stage III or IV HIV infection.
- Provide informed consent.
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions or symptoms are excluded:
- Kaposi's sarcoma lesions in the proposed treatment sites.
- Liable to require radiation or chemotherapy during the course of the study.
- Not likely to survive the length of the study.
- Obvious ultra-violet-irradiated skin damage in the treatment areas and anyone with recent UV exposure or likely to have such exposure (e.g.:
- holiday tans obtained in Hawaii, members of UV box tanning salons, etc.) Allergy to lidocaine.
Concurrent Medication:
Excluded:
- Other Immunomodulators.
Concurrent Treatment:
Excluded:
- Radiation.
Patients with the following are excluded:
- Kaposi's sarcoma lesions in the proposed treatment sites.
- Liable to require radiation or chemotherapy during the course of the study.
- Not likely to survive the length of the study.
- Obvious ultra-violet-irradiated skin damage in the treatment areas.
- Allergy to lidocaine.
Prior Medication:
Excluded:
- Prior DNCB therapy.
Contacts and Locations
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00002031 History of Changes |
| Other Study ID Numbers: | 047A |
| Study First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by NIH AIDS Clinical Trials Information Service:
|
Langerhans Cells Dinitrochlorobenzene Acquired Immunodeficiency Syndrome AIDS-Related Complex |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases |
Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |
ClinicalTrials.gov processed this record on June 18, 2013