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
| Type | Name | Description |
|---|---|---|
| DRUG | N Acetylcysteine | 1200 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.