MedPath

A pilot study for universal testing and treatment of Latent Tuberculosis Infection (LTBI)

Phase 4
Completed
Conditions
atent Tuberculosis Infection
Latent Tuberculosis Infection
Respiratory - Other respiratory disorders / diseases
Infection - 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
NameTimeMethod
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
NameTimeMethod
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