CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 322 enrolled
Drug / intervention
Rifaximindrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00686920
NCT00686920Phase 3Completed

A Multi-Center, Open-Label Trial to Evaluate the Long-Term Safety and Tolerability of Rifaximin 550 mg BID in Subjects With a History of Hepatic Encephalopathy

Bausch Health Americas, Inc.·interventional·Posted May 30, 2008·Updated Aug 14, 2019

In Brief

A Phase 3 clinical trial evaluating Rifaximin for Hepatic Encephalopathy. Completed, enrolled 322 participants across 35 sites in 2 countries.

Detailed Summary

This study will look at the safety of a drug used in participants who have had hepatic encephalopathy (HE) in the past.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States
Collaborators--

Timeline

Phase 3CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 30, 2008
Enrollment StartMar 7, 2007
Primary CompletionDec 8, 2010
TodayJul 2, 2026
Enrollment to primary: 3.8 yearsPosted 18.1 years ago

Interventions

Rifaximindrug

Oral