Actively Recruiting
Diagnostic and Therapeutic Applications in Microarrays in Organ Transplantation
Led by University of Alberta · Updated on 2026-01-29
500
Participants Needed
26
Research Sites
839 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Diagnostic and Therapeutic Applications in Microarrays in Organ Transplantation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Kidney transplant recipients aged 18 years or older undergoing a kidney biopsy for clinical reasons as determined by their physician or surgeon
You will not qualify if you...
- Patients who decline participation or are unable to give informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 26 locations
1
University of Alabama
Birmingham, Alabama, United States, 35294-0006
Completed
2
University of Maryland School of Medicine
Baltimore, Maryland, United States, 21209
Completed
3
University of Michigan Health System
Ann Arbor, Michigan, United States, 48109-5395
Completed
4
University of Minnesota
Minneapolis, Minnesota, United States, 55455
Completed
5
Barnes-Jewish Hospital
St Louis, Missouri, United States, 63110
Completed
6
Montefiore Medical Center
The Bronx, New York, United States
Completed
7
Pinnacle Transplant Associates
Harrisburg, Pennsylvania, United States
Completed
8
Texas Transplant Institute - Methodist Healthcare System
San Antonio, Texas, United States, 78229
Completed
9
Virginia Commonwealth University School of Medicine
Richmond, Virginia, United States, 23298
Completed
10
University of Wisconsin School of Medicine and Public Health
Madison, Wisconsin, United States, WI 53705
Completed
11
Medical University of Vienna
Vienna, Austria
Actively Recruiting
12
Department of Medicine, University of Alberta
Edmonton, Alberta, Canada, T6G 2S2
Actively Recruiting
13
University of British Columbia, St. Paul's Hospital
Vancouver, British Columbia, Canada
Withdrawn
14
University Hospital Merkur
Zagreb, Croatia
Completed
15
Institute for Experimental and Clinical Medicine (IKEM)
Prague, Czechia
Actively Recruiting
16
Hopital Necker
Paris, France
Completed
17
Hopital St. Louis
Paris, France
Completed
18
Charité - Universitätmedizin Berlin
Berlin, Germany
Completed
19
Medizinische Hochschule
Hanover, Germany, 30625
Completed
20
Beaumont Hospital
Dublin, Ireland
Withdrawn
21
Pomeranian Medical University in Szczecin
Szczecin, Poland
Completed
22
University of Ljubljana
Ljubljana, Slovenia
Completed
23
Department of Surgery, University of Usan, College of Medicine
Seoul, South Korea, 05505
Completed
24
Vall d'Hebron Hospital
Barcelona, Spain, 08035
Completed
25
University Hospital Zurich
Zurich, Switzerland, 8091
Completed
26
Manchester Royal Infirmary
Manchester, United Kingdom, M13 9WL
Completed
Research Team
P
Philip F Halloran, MD PhD
CONTACT
K
Konrad S Famulski, PhD DSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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