The impact of human immunodeficiency virus infection on drug-resistant tuberculosis.
F M Gordin, E T Nelson, J P Matts...
https://pubmed.ncbi.nlm.nih.gov/8912768Completed
Age: 1Day +
All Genders
ID00000785
A Registry of Tuberculosis Cases in the CPCRA
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2013-10-01
1509
Participants Needed
13
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
PRIMARY: To estimate the proportion of tuberculosis patients in the CPCRA who have drug-resistant tuberculosis (TB) and to describe the patterns of drug resistance. SECONDARY: To compare drug resistance data on the Mycobacterium tuberculosis isolates of HIV-infected patients to those of HIV-uninfected patients who are being followed in the CPCRA. To assess the relationship of resistance data with geographic, demographic, and HIV and TB risk factor information. Geographic areas and demographic subgroups affected by the TB epidemic appear to be congruent and associated with the concurrent HIV epidemic. The total number of CPCRA patients who will develop, or who have experienced, confirmed TB is unknown. It is critical to determine the depth and breadth of the current problem of drug-resistant TB.
CONDITIONS
Official Title
A Registry of Tuberculosis Cases in the CPCRA
Who Can Participate
Age: 1Day +
All Genders
Eligibility Criteria
You may qualify if you...
Patients must meet the following criteria:
- CPCRA patients with confirmed pulmonary or extrapulmonary TB. Confirmed clinical TB requires a positive culture for Mycobacterium tuberculosis.
NOTE:
- There is no requirement that patients have HIV infection.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Trial Site Locations
Total: 13 locations
1
Denver CPCRA / Denver Public Hlth
Denver, Colorado, United States, 80204
Status Unknown
2
Veterans Administration Med Ctr / Regional AIDS Program
Washington D.C., District of Columbia, United States, 20422
Status Unknown
3
AIDS Research Alliance - Chicago
Chicago, Illinois, United States, 60657
Status Unknown
4
Louisiana Comm AIDS Rsch Prog / Tulane Univ Med
New Orleans, Louisiana, United States, 70112
Status Unknown
5
Comprehensive AIDS Alliance of Detroit
Detroit, Michigan, United States, 48201
Status Unknown
6
Henry Ford Hosp
Detroit, Michigan, United States, 48202
Status Unknown
7
North Jersey Community Research Initiative
Newark, New Jersey, United States, 07103
Status Unknown
8
Addiction Research and Treatment Corp
Brooklyn, New York, United States, 11201
Status Unknown
9
Clinical Directors Network of Region II
New York, New York, United States, 10011
Status Unknown
10
Harlem AIDS Treatment Group / Harlem Hosp Ctr
New York, New York, United States, 10037
Status Unknown
11
Bronx Lebanon Hosp Ctr
The Bronx, New York, United States, 10456
Status Unknown
12
Portland Veterans Adm Med Ctr / Rsch & Education Grp
Portland, Oregon, United States, 97210
Status Unknown
13
Richmond AIDS Consortium
Richmond, Virginia, United States, 23298
Status Unknown
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How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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