Monitoring liver transplant recipients for early detection of complications
Official title: Proteogenomic Monitoring and Assessment of Liver Transplant Recipients
Run by Northwestern University · NCT01644903 · Data updated 2026-11-12
This study is testing if checking blood, urine, and tissue samples from liver transplant patients can help spot early signs of kidney problems, organ rejection, and Hepatitis C to improve their treatment and health outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Northwestern University Academic / other |
| Locations | 1 site (Chicago, Illinois) |
| Status | Recruiting |
| Started | April 2010 |
| Main results expected | December 2030 |
| Study ends | December 2031 |
| Registry record updated | May 22, 2026 |
| Trial ID | NCT01644903 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older who are undergoing liver transplantation, whether from living or deceased donors.
✕Probably not a fit
Patients who are unable or unwilling to provide informed consent will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to analyze blood, urine, and tissue samples from liver transplant recipients to identify early signs of Chronic Kidney Disease (CKD), Acute Rejection (AR), and Hepatitis C Virus (HCV). By utilizing advanced molecular techniques and biomarkers, the study seeks to improve the sensitivity and specificity of early detection compared to traditional methods. The goal is to enhance treatment outcomes and potentially reduce the need for repeat organ transplants through timely intervention.
Why it matters
Potential benefit: If successful, this study could lead to earlier detection and treatment of complications in liver transplant recipients, improving their overall health and longevity.
How similar studies have gone: Previous studies have shown promise in using molecular techniques for early detection of transplant complications, indicating a potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Male and female recipients of all races, ≥18 years of age. 2. Patients undergoing primary or subsequent living or deceased donor liver transplantation. 3. Subject and/or guardian must be able to provide informed consent. 4. Subject and/or guardian must be able to comply with the study protocol. Exclusion Criteria: 1\. Inability or unwillingness of a participant and/or guardian to provide informed consent.
Where it's running
-
Northwestern Memorial Hospital
Chicago, Illinois, United States Recruiting
Study contacts
- Principal investigator: Josh Levitsky, MD — Northwestern University
- Study coordinator: Misael Villegas, BA
- Email: misael.villegas@northwestern.edu
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.