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Invasive Monitoring Attenuation Through Gene Expression (IMAGE) Trial
This study is designed to evaluate the safety and efficacy of a leukocyte gene expression profiling method in the monitoring of asymptomatic heart transplant patients for acute rejection.
Cardiac allograft rejection is experienced by 20-50% of patients at least once during the first year after cardiac transplantation under the present immunosuppression regimens. With a higher incidence of acute cellular rejection (ACR) in the first six months post-transplant, ACR continues to occur beyond the first year post-transplant. However, the optimal strategy for detecting rejection during this period of lower risk period for ACR is still controversial. The standard for rejection surveillance has been the endomyocardial biopsy (EMB). However, EMB is invasive, causes morbidity, and is subject to sampling error and inter-observer variability. Gene expression profiling (GEP), with its high negative predictive value (NPV) for acute cellular rejection (ACR), appears to be well suited to identify low-risk patients who can be safely managed without routine invasive endomyocardial biopsy (EMB).
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
VA Palo Alto Health Care System
Palo Alto, California, United States
Stanford University Medical Center
Stanford, California, United States
Northwestern University
Chicago, Illinois, United States
University of Chicago
Chicago, Illinois, United States
Mid America Heart Institute - St. Luke's Hospital
Kansas City, Missouri, United States
Barnes Jewish Hospital - Washington University
St Louis, Missouri, United States
Newark Beth Israel Medical Center
Newark, New Jersey, United States
Columbia University Medical Center - New York Presbyterian Hospital
New York, New York, United States
The Cleveland Clinic
Cleveland, Ohio, United States
University of Pennsylvania
Philadelphia, Pennsylvania, United States
Start Date
January 1, 2005
Completion Date
October 1, 2009
Last Updated
November 20, 2009
629
ACTUAL participants
AlloMap molecular expression testing
DEVICE
Right ventricular endomyocardial biopsy
PROCEDURE
Lead Sponsor
XDx
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06788275