MedPath

use of acetyl cystein in prevention of anti-TB drug induced hepatitis

Not Applicable
Conditions
drug induced hepatits.
Toxic liver disease with hepatic necrosis
Registration Number
IRCT201205259855N1
Lead Sponsor
Arak University of Medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

age over 50 years; hemodynamic stability (mean arterial blood pressure >70 mmHg or systolic blood pressure >90mmHg ) Exclusion criteria: history of acute or chronic renal and liver failure accordance with the definitions of relevant, Unavailability of information related to liver function in basic mode, use of N- acetylcysteine orally, injected or inhaled during 1 month before the beginning of the study; Experience has confirmed that the incidence of hypersensitivity reactions following oral, intravenous or inhaled N- acetylcysteine; receiving concomitant drugs or compounds with antioxidant effects such as vitamin C, vitamin E; HIV + patients; use of alcohol

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
iver enzym and if necessary bilirubin. Timepoint: start of treatment and end of first , second, third and fourth of treatment. Method of measurement: paraclinic measurement and clinical interview.
Secondary Outcome Measures
NameTimeMethod
Decrease of ESR and CRP. Timepoint: start of tretment and end of first , second,third , fourth of tretment. Method of measurement: lESR and CRP measurement.
© Copyright 2025. All Rights Reserved by MedPath