Clinical Trial

ROLE OF N-ACETYLCYSTEINE IN NON-ACETAMINOPHEN-INDUCED LIVER FAILURE

Recruiting
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Summary
This randomized controlled trial evaluates whether oral N-acetylcysteine (NAC), given alongside standard supportive care, improves survival and reduces mortality in patients with non-acetaminophen-induced acute liver failure (ALF), compared to supportive care alone. Secondary objectives are to assess NAC's effect on length of hospital stay and improvement in liver function tests. Sixty-two adult patients (18-60 years) will be randomized 1:1 to NAC or control, with outcomes assessed at 28 days (survival/mortality) and day 4 (liver function tests).
Trial Details
NCT Number NCT07765823
Lead Sponsor King Edward Medical University
Conditions Acute Liver Failure, Non-acetaminophine Induced Liver Failure
Enrollment 62 participants
Start Date 2026-07-16
Primary Completion 2026-10-15 (estimated)
Study Completion 2026-10-17 (estimated)
Updated on ClinicalTrials.gov 2026-08-14