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Clinical Trials in Canada / NCT05242315
Recruiting Phase 4

Extended-Release Tacrolimus Following Liver Transplantation

NCT05242315 · tracked via the Priya Life Science Canada tracker
Phase
Phase 4
Started
2022-05-15
Last updated
2026-09-15

Condition(s) studied

Liver Transplant; ComplicationsRenal InsufficiencyImmunosuppressant Adverse ReactionMetabolic SyndromeCardiovascular Diseases

Investigational drug(s) / intervention(s)

Envarsus Oral ProductPrograf (SOC) →

Envarsus Oral Product: as described in arm/group description

Prograf (SOC): Prograf (SOC)

Study 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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: \- Adult individuals transplanted at the University of Alberta Exclusion Criteria: * 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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Univerity of Alberta Edmonton Alberta Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05242315 on ClinicalTrials.gov ↗ ← All trials in Canada