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Clinical Trial Summary

Intervention - Subjects will be randomized to 2 groups

Group A - subjects will receive Prednisolone for 20 days with NAC (N-Acetylcysteine)

Group B - will receive NAC (N-Acetylcysteine) only NAC (N-acetylcysteine) dosing

Loading dose: 150 mg/kg IV; mix in 200 mL of 5% dextrose in water (D5W) and infuse over 1 hour

Dose 2: 50 mg/kg IV in 500 mL D5W over 4 h

Dose 3: 100 mg/kg IV in 1000 mL D5W over 16 h

- Monitoring and assessment-Liver Biopsy at baseline and at 3 months, Liver Function Test at regular intervals.

- Stopping rule-Development of sepsis, worsening of Liver functions.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02686385
Study type Interventional
Source Institute of Liver and Biliary Sciences, India
Contact
Status Terminated
Phase N/A
Start date March 1, 2016
Completion date August 31, 2016

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