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NCT04727320

The Clinical Application of Tauroursodeoxycholic Acid in Patients With Liver Fibrosis.

Status unknown EARLY_PHASE1 Last updated 9 March 2021
What this trial tests

EARLY_PHASE1 trial testing Tauroursodeoxycholic acid in Liver Cirrhosis in 60 participants. Status unknown.

Timeline
5 March 2021
Primary endpoint
30 July 2021
30 July 2021

Quick facts

Lead sponsorThe First Affiliated Hospital with Nanjing Medical University
PhaseEARLY_PHASE1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment60
Start date5 March 2021
Primary completion30 July 2021
Estimated completion30 July 2021

Drugs / interventions tested

Conditions studied

Sponsor

The First Affiliated Hospital with Nanjing Medical University

Who can join

Adults 30 to 60, any sex, with Liver Cirrhosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a prospective study. We signed an informed consent form with patients with liver fibrosis and took tauroursodeoxycholic acid orally for half a year. After half a year, liver biopsy was performed using histopathology, immunohistochemistry, and polymerase chain reaction, Western blotting method was used to determine the expression level of fibrosis-related markers to verify the effect of taurodeoxycholic acid on patients with liver fibrosis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Tauroursodeoxycholic acid

Trials testing the same drug.

Other recruiting trials for Liver Cirrhosis

Currently open trials in the same condition.

Other The First Affiliated Hospital with Nanjing Medical 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/NCT04727320.

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