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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)

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Dinitrochlorobenzene
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Langerhans Cells, Dinitrochlorobenzene, Acquired Immunodeficiency Syndrome, AIDS-Related Complex

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • San Francisco AIDS Clinic / San Francisco Gen Hosp

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
June 23, 2005
Sponsor
University of California, San Francisco
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1. Study Identification

Unique Protocol Identification Number
NCT00002031
Brief 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)
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)
Study Type
Interventional

2. Study Status

Record Verification Date
February 1990
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of California, San Francisco

4. Oversight

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Langerhans Cells, Dinitrochlorobenzene, Acquired Immunodeficiency Syndrome, AIDS-Related Complex

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Dinitrochlorobenzene

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility 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.
Facility Information:
Facility Name
San Francisco AIDS Clinic / San Francisco Gen Hosp
City
San Francisco
State/Province
California
ZIP/Postal Code
941102859
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
1769706
Citation
Stricker RB, Elswood BF. Dendritic cells and dinitrochlorobenzene (DNCB): a new treatment approach to AIDS. Immunol Lett. 1991 Aug;29(3):191-6. doi: 10.1016/0165-2478(91)90169-b. Erratum In: Immunol Lett 1992 Aug;33(3):316.
Results Reference
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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)

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