Diagnostic and Therapeutic Applications of Microarrays in Liver Transplantation

Description

INTERLIVER is a prospective observational study of the relationship of the molecular phenotype of 300 liver transplant biopsies to the histologic phenotype and the clinical features and outcomes. A segment of a biopsy performed as standard-of-care for indications, or by center protocol, will be used for gene expression study.

Conditions

Liver Dysfunction

Study Overview

Study Details

Study overview

INTERLIVER is a prospective observational study of the relationship of the molecular phenotype of 300 liver transplant biopsies to the histologic phenotype and the clinical features and outcomes. A segment of a biopsy performed as standard-of-care for indications, or by center protocol, will be used for gene expression study.

Diagnostic and Therapeutic Applications of Microarrays in Liver Transplantation, a Multicenter Study

Diagnostic and Therapeutic Applications of Microarrays in Liver Transplantation

Condition
Liver Dysfunction
Intervention / Treatment

-

Contacts and Locations

San Francisco

University of California San Francisco, Transplant Research Unit, San Francisco, California, United States, 94143

Chicago

Northwestern Memorial Hospital, Chicago, Illinois, United States, 60611

Baltimore

University of Maryland School of Medicine, Baltimore, Maryland, United States, 21201

Detroit

Henry Ford Transplant Institute, Detroit, Michigan, United States, 48202

Nashville

Vanderbilt University Medical Center, Vanderbilt Transplant Center, Nashville, Tennessee, United States, 37232

Dallas

Baylor University Medical Center, Annette C. and Harold C. Simmons Transplant Institute, Dallas, Texas, United States, 75246

Richmond

Transplant Surgery, VCU Medical Center, Richmond, Virginia, United States, 23298

Seattle

Division of Transplant Surgery, University of Washington, Seattle, Washington, United States, 98195

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * biopsy for clinical indications
  • * no consent, pregnant women

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Alberta,

Philip F Halloran, MD, PhD, PRINCIPAL_INVESTIGATOR, University of Alberta

Study Record Dates

2026-12