Clinical Trials Directory

Trials / Completed

CompletedNCT00564642

Investigation of the Effect of N Acetylcysteine Against Anti-Tuberculosis Drugs Induced Liver Toxicity

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
National Research Institute of Tuberculosis and Lung Disease, Iran · Other Government
Sex
All
Age
60 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Tuberculosis is one of the major health problems in developing countries. Isoniazid, rifampin and pyrazinamide, the first line drugs used for tuberculosis chemotherapy, are associated with hepatotoxicity. The rate of hepatotoxicity has been reported to be much higher in developing countries compared to that in advanced countries with a similar dose schedule. Oxidative stress has proposed as one of the mechanisms responsible for anti-tuberculosis drugs induced hepatic injury. The oxidative stress is closely associated with decrease of glutathione levels. In the present study N acetylcysteine, a precursor of glutathione, was investigated for hepatoprotective effect against anti-tuberculosis drugs induced liver injury.

Conditions

Interventions

TypeNameDescription
DRUGN Acetylcysteine1200 mg, BD, 2weeks

Timeline

Start date
2007-11-01
Primary completion
2009-01-01
Completion
2009-04-01
First posted
2007-11-28
Last updated
2009-04-22

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT00564642. Inclusion in this directory is not an endorsement.