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NCT06236165

Clinical Study Evaluating Efficacy, Safety and Molecular Mechanism of N-acetylcysteine Supplementation in Patients With Hepatic and Post Hepatic Jaundice

Completed Phase 2 Last updated 30 July 2025
What this trial tests

Phase 2 trial testing N-acetylcysteine in Hepatic and Post Hepatic Jaundice in 44 participants. Completed in 22 January 2025.

Timeline
14 February 2024
Primary endpoint
22 January 2025
22 January 2025

Quick facts

Lead sponsorTanta University
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment44
Start date14 February 2024
Primary completion22 January 2025
Estimated completion22 January 2025
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Tanta University

Who can join

Adults 18 to 70, any sex, with Hepatic and Post Hepatic Jaundice. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Investigating the efficacy, safety, and molecular mechanism of N-acetylcysteine supplementation in improving elevated direct bilirubin level and liver function tests in patients with hepatic and post-hepatic jaundice.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of N-acetylcysteine

Trials testing the same drug.

Other Tanta University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06236165.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing