Double blind, placebo-controlled, randomised clinical trial to evaluate the efficacy of co-trimoxazole given as prophylaxis in reducing mortality in human immunodeficiency virus-infected adults with tuberculosis
Completed
- Conditions
- Tuberculosis and HIV/AIDSInfections and InfestationsTuberculosis
- Registration Number
- ISRCTN15281875
- Lead Sponsor
- niversity College London (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 1045
Inclusion Criteria
1. Adults greater than 16 years old
2. HIV-infected
3. Newly diagnosed pulmonary tuberculosis
4. Had a permanent residential address
5. Not pregnant
6. Willing to give informed consent
Exclusion Criteria
1. Pregnant
2. Terminally ill World Health Organization (WHO) stage 4 patients
3. History of sulfonamide allergy
4. Already receiving co-trimoxazole
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method