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Clinical Trial ● Currently Recruiting NCT03193151

Diagnostic and Therapeutic Applications of Microarrays in Liver Transplantation

Diagnostic and Therapeutic Applications of Microarrays in Liver Transplantation — Recruiting • Gastroenterology • NCT03193151.

📅 04 Jun 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
NCT ID
NCT03193151
Sponsor
University of Alberta
Start
2017-12-19
ClinicaliQ Trial Snapshot
  • Diagnostic and Therapeutic Applications of Microarrays in Liver Transplantation — Recruiting • Gastroenterology • NCT03193151.
  • What is being tested: INTERLIVER evaluates whether microarray analysis of liver transplant biopsies can identify molecular patterns that correlate with histological findings and predict clinical outcomes, potentially improving diagnostic accuracy beyond standard histopathology alone.
  • Patient eligibility overview: The study includes 300 liver transplant recipients undergoing clinically indicated biopsies for standard-of-care diagnostic purposes, with biopsy segments retained for molecular microarray analysis alongside routine histological assessment.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

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.

Eligibility Snapshot
  • : * biopsy for clinical indications

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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