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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01525797
Other study ID # 002-197
Secondary ID
Status Active, not recruiting
Phase N/A
First received May 11, 2011
Last updated March 13, 2015
Start date October 2002
Est. completion date November 2015

Study information

Verified date March 2015
Source Baylor Research Institute
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardUnited States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The purpose of this study is to see what a lab test will show and if there is a way to predict which patients will be more likely to have rejection after receiving a liver transplant.


Description:

The purpose of this study is simply to see what the new oligonucleotide microarrays will show when comparing the the different patient groups. The results of this study will be one of the first steps In exploring the potential use of this new test.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 200
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 17 Years to 65 Years
Eligibility Inclusion Criteria:

- Received a liver Transplant

Exclusion Criteria:

- Received Multiple Organ Transplant

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Baylor University Medical Center Dallas Texas

Sponsors (1)

Lead Sponsor Collaborator
Baylor Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Identify signatures predictive of graft rejection or tolerance. Analyze the pattern of gene expression in patients undergoing solid organ transplantation 2 years No
See also
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Completed NCT00275639 - The Effects of Angiotensin II Receptor Blockade on Kidney Function and Scarring After Liver Transplant Phase 4
Completed NCT01672164 - Discovery and Validation of Proteogenomic Biomarker Panels in Liver Transplant Recipients N/A
Completed NCT01638559 - Immunosuppression Withdrawal for Stable Pediatric Liver Transplant Recipients Phase 2
Recruiting NCT06418893 - Effect of TCI Propofol on Liver Transplant (TCI) Propofol on Intra-operative Usage of Vasopressors in Liver Transplant Recipients. Phase 2/Phase 3