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Clinical Trial Summary

Determine the levels of Donor-derived (dd)cell-free DNA(cfDNA )in liver transplant recipients with normal liver function tests (LFTs) indicating stable immunosuppression status (IS). Based on this range use the dd-cfDNA levels to determine over or under IS in liver transplant patients to make changes to their IS medication regimen.


Clinical Trial Description

dd-cfDNA is a non-invasive method to measure graft function stability in liver transplant patients. Liver biopsy is the standard to determine liver rejection and graft function, but no tests exist currently to be able to help guide the IS regimen in these patients. LFTs are not as specific to determine graft function hence testing dd-cfDNA levels can help guide the Immunosuppression (IS )medications dosing and help identify rejection early. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06225206
Study type Observational
Source Methodist Health System
Contact Kavya Vinod Mankulangara, PharmD
Phone 214-947-4681
Email MHSIRB@mhd.com
Status Recruiting
Phase
Start date July 1, 2021
Completion date December 31, 2024

See also
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Active, not recruiting NCT03815864 - Antibodies and Liver Retransplantation
Recruiting NCT05361044 - Liver Graft Viability Assessment During Normothermic Regional Perfusion N/A
Recruiting NCT05866796 - Serum GLYcomics to Predict Graft Loss and Mortality After Liver Transplantation
Active, not recruiting NCT03396016 - Plasmatic Factor V as a Predictor of Graft Dysfunction After Liver Transplantation