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Protective effect of N-acetylcysteine on INH-induced hepatotoxicity in patients with latent TB.

Phase 3
Recruiting
Conditions
atent tuberculosis.
Latent tuberculosis
Z22.7
Registration Number
IRCT20200328046886N4
Lead Sponsor
Mazandaran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
72
Inclusion Criteria

Patients diagnosed with latent tuberculosis using tuberculin skin test or IGRA.

Exclusion Criteria

Liver disease
Active tuberculosis
hepatitis
Pregnansy
Lactating
Alcoholism
Sensitivity to NAC

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Age. Timepoint: The beginning of the study. Method of measurement: questionnaire.;Sex. Timepoint: The beginning of the study. Method of measurement: questionnaire.;AST. Timepoint: The beginning ,first ,second,forth ,sixth, eighth weeks of the study. Method of measurement: Labrotory.;ALT. Timepoint: The beginning ,first ,second,forth ,sixth, eighth weeks of the study. Method of measurement: Labrotory.;Drug side effects. Timepoint: Start until the end of the study. Method of measurement: questionnaire.;ALP. Timepoint: The beginning and end of the study. Method of measurement: Labratory.;Bilirubin total. Timepoint: The beginning and end of the study. Method of measurement: Labratory.
Secondary Outcome Measures
NameTimeMethod
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