Study of Liver Transplant For End-Stage Liver Disease Caused By Chronic Hepatitis C Infection

NCT00163657 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 312

Last updated 2017-01-12

Study results available
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Summary

The purpose of this study is to compare three treatment regimens in patients who have received a liver transplant for end-stage liver disease caused by Chronic Hepatitis C infection.

Conditions

  • End Stage Liver Disease
  • Hepatitis C

Interventions

DRUG

Daclizumub

anti-rejection drug

DRUG

Tacrolimus

anti rejection drug

DRUG

Cyclosporine

anti rejection drug

DRUG

MMF

anti rejection drug

Sponsors & Collaborators

  • Baylor Health Care System

    collaborator OTHER
  • Emory University

    collaborator OTHER
  • University of Southern California

    collaborator OTHER
  • Mayo Clinic - Scottsdale/Phoenix, Arizona

    collaborator UNKNOWN
  • New York Presbyterian Hospital

    collaborator OTHER
  • Oregon Health and Science University

    collaborator OTHER
  • New York University

    collaborator OTHER
  • University of Cincinnati

    collaborator OTHER
  • University of Alabama at Birmingham

    collaborator OTHER
  • The University of Texas Health Science Center at San Antonio

    collaborator OTHER
  • University of Chicago

    collaborator OTHER
  • University of California, San Francisco

    collaborator OTHER
  • Mayo Clinic - Rochester, Minnesota

    collaborator UNKNOWN
  • Medical University of South Carolina

    collaborator OTHER
  • University of Virginia

    collaborator OTHER
  • Lahey Clinic

    collaborator OTHER
  • University of Medicine and Dentistry of New Jersey

    collaborator OTHER
  • Northwestern Memorial Hospital

    collaborator OTHER
  • Baylor Research Institute

    lead OTHER

Principal Investigators

  • Goran Klintmalm, MD · Baylor Univeristy Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-07-31
Primary Completion
2006-04-30
Completion
2007-01-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00163657 on ClinicalTrials.gov