A pilot study for universal testing and treatment of Latent Tuberculosis Infection (LTBI)
Phase 4
Completed
- Conditions
- atent Tuberculosis InfectionLatent Tuberculosis InfectionRespiratory - Other respiratory disorders / diseasesInfection - Other infectious diseases
- Registration Number
- ACTRN12619001439134
- Lead Sponsor
- Woolcock Institute of Medical Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 2834
Inclusion Criteria
Resident in any of three selected Aps in Ca Mau Province, Vietnam
Exclusion Criteria
Exclusion criteria for the TEST phase;
No exclusion criteria for the test phase.
Exclusion criteria for the TREAT phase;
* Pregnant women or women planning and attempting to fall pregnant
* Active TB
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of eligible patients who complete at least 80% of doses of the required treatment, via record of drug delivery (directly observed therapy)[18 weeks from treatment initiation for RIF regimen and 12 weeks from treatment initiation for 3HP regimen]
- Secondary Outcome Measures
Name Time Method