Liver Transplant Clinical Trials

Clinical trials related to Liver Transplant Procedure

Use of Transient Elastography to Guide Immunosuppression Minimization Post Liver Transplantation

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Following Liver transplantation, recipients remain on life long immunosuppression. Prolonged exposure to immunosuppression is associated with side effects and complications including kidney dysfunction, diabetes, heart disease and cancer risk. Therefore studies are looking at safe ways to reduce or stop immunosuppression. An individual without autoimmune liver disease (these patients are at higher risk of rejection), without history of rejection, with normal blood tests (liver biochemistry, liver function, etc.) can be eligible for minimization of immunosuppression. A recent study showed use of fibroscan (an Ultrasound, which provides information on liver stiffness (diseased liver is hard while a normal liver is soft) and fat content) provides more objective information to help investigators select individuals who will tolerate immunosuppression minimization. Our goal is to see if use of fibroscan allows the investigators to safely minimize immunosuppression in eligible individuals. The secondary aims are to assess benefit on kidney function, heart disease and risk factors for heart disease.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 2 years or more post-liver transplant

• 18 years or older

Locations
Other Locations
Canada
University of Alberta
RECRUITING
Edmonton
Time Frame
Start Date: 2025-12-01
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 50
Treatments
No_intervention: Standard of Care
Followed per standard of care
Experimental: Immunosuppression minimization
will have immunosuppression reduction during the study using fibroscan
Related Therapeutic Areas
Sponsors
Leads: University of Alberta

This content was sourced from clinicaltrials.gov