Clinical Trial Details

Trial ID: L0675
Source ID: JPRN-UMIN000004034
Associated Drug: Ursodeoxycholic acid
Title:
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Nonalcoholic steatohepatitis (NASH)
Interventions: Administration of ursodeoxycholic acid (600mg/day)for 52 weeks <br>Administration of ursodeoxycholic acid (1200mg/day)for 52 weeks
Outcome Measures: 1) Histological change in liver biopsies<br>2) Functional change in liver enzymes<br>3) Safetynan
Sponsor/Collaborators: Division of Gastroenterology, Saiseikai Suita Hospital
Gender: All
Age: 20years-oldNot applicable
Phases: Not applicable
Enrollment: 60
Study Type: Interventional
Study Designs: Parallel Randomized
Start Date: 13/08/2010
Completion Date: --
Results First Posted: --
Last Update Posted: 2 April 2019
Locations: Japan
URL: https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000004852