RecruitingNCT01299168

Diagnostic and Therapeutic Applications in Microarrays in Organ Transplantation

Multi-centric Observational Study to Analyse the Diagnostic Molecular Features in the Clinical Setting of Kidney Allograft Biopsies


Sponsor

University of Alberta

Enrollment

500 participants

Start Date

May 1, 2011

Study Type

OBSERVATIONAL

Conditions

Summary

The current standard for biopsy-based diagnoses of dysfunction of kidney transplants is the Banff Classification which represents arbitrary international consensus. Recent data-driven approaches using molecular and conventional technologies indicate that mere consensus produces frequently incorrect diagnoses with potential harm to patients due to inappropriate treatment. To address this unmet need and improve diagnostics in the area of organ transplantation, the Alberta Transplant Applied Genomics Centre (ATAGC) has developed a new diagnostic system that combines the molecular and histopathological features of transplant biopsies, plus clinical and laboratory parameters, to create the first Integrated Diagnostic System. The present study will validate and refine this system in 500 prospectively unselected biopsies for clinical indications from American, Canadian and European centres in addition to 300 biopsies already collected. Due to a considerable interest and support from participating Centers, the study is further extended to 1500 prospective biopsies. Thus this is the extension of the INTERCOM study (INTERCOMEX). In addition to demonstrating the feasibility and value of this System in routine patient care and clinical trials, the study will develop and optimize a transparent and user-friendly reporting format to communicate this information to clinicians and obtain detailed feedback on how this system can best improve patient care.


Eligibility

Min Age: 18 Years

Inclusion Criteria1

  • All kidney transplant recipients ≥18yrs of age undergoing a kidney biopsy for clinical indications, as determined by their physician or surgeon, will be eligible to enrol in the study.

Exclusion Criteria1

  • Patients will be excluded from the study if they decline participation or are unable to give informed consent.

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(26)

University of Alabama

Birmingham, Alabama, United States

University of Maryland School of Medicine

Baltimore, Maryland, United States

University of Michigan Health System

Ann Arbor, Michigan, United States

University of Minnesota

Minneapolis, Minnesota, United States

Barnes-Jewish Hospital

St Louis, Missouri, United States

Montefiore Medical Center

The Bronx, New York, United States

Pinnacle Transplant Associates

Harrisburg, Pennsylvania, United States

Texas Transplant Institute - Methodist Healthcare System

San Antonio, Texas, United States

Virginia Commonwealth University School of Medicine

Richmond, Virginia, United States

University of Wisconsin School of Medicine and Public Health

Madison, Wisconsin, United States

Medical University of Vienna

Vienna, Austria

Department of Medicine, University of Alberta

Edmonton, Alberta, Canada

University of British Columbia, St. Paul's Hospital

Vancouver, British Columbia, Canada

University Hospital Merkur

Zagreb, Croatia

Institute for Experimental and Clinical Medicine (IKEM)

Prague, Czechia

Hopital Necker

Paris, France

Hopital St. Louis

Paris, France

Charité - Universitätmedizin Berlin

Berlin, Germany

Medizinische Hochschule

Hanover, Germany

Beaumont Hospital

Dublin, Ireland

Pomeranian Medical University in Szczecin

Szczecin, Poland

University of Ljubljana

Ljubljana, Slovenia

Department of Surgery, University of Usan, College of Medicine

Seoul, South Korea

Vall d'Hebron Hospital

Barcelona, Spain

University Hospital Zurich

Zurich, Switzerland

Manchester Royal Infirmary

Manchester, United Kingdom

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT01299168