RecruitingPhase 4NCT05242315

Extended-Release Tacrolimus Following Liver Transplantation

Feasibility, Efficacy And Safety Of De Novo Extended-Release Tacrolimus Following Liver Transplantation


Sponsor

University of Alberta

Enrollment

94 participants

Start Date

May 15, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Medications used after transplant to prevent rejection are associated with many side effects. Tacrolimus side effects include kidney dysfunction; tremor, headaches, difficulty sleeping, change in sensation (legs), seizure, or confusion; high blood pressure; anemia, or low blood cell counts; diabetes; abnormal cholesterol and weight gain. The investigators want to use a new, approved, formulation of the standard medication (Envarsus) as they believe it may be associated with reduced side effects. The investigators would like to assess how safe it is to use this medication and how well it works in comparison to currently used formulations. The investigators will study if there are less side effects and will study clinical outcomes (including how well the liver does and if there is need for hospitalizations after transplant). The investigators hope that this information will improve the care provided to and outcomes in patients following liver transplant.


Eligibility

Min Age: 18 Years

Inclusion Criteria1

  • \- Adult individuals transplanted at the University of Alberta

Exclusion Criteria5

  • Individuals with congenital long QT syndrome
  • Patients with elevated bilirubin \> 100 umol/L post-LT (at day 3)
  • Patients with chronic kidney disease (eGFR \< 45 ml per minute per 1.73 m2)
  • Patients with acute kidney injury requiring discontinuation of calcineurin inhibitors.
  • Patients who have hepatocellular carcinoma, require a re-transplant, or receive multi-visceral transplant

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Interventions

DRUGEnvarsus Oral Product

as described in arm/group description

DRUGPrograf (SOC)

Prograf (SOC)


Locations(1)

Univerity of Alberta

Edmonton, Alberta, Canada

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NCT05242315


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