🏛️ Verified NIH Record • Updated 2025-04-11

Calcineurin Inhibitor in NEuRoloGically Deceased Donors to Decrease Kidney delaYed Graft Function (CINERGY) (NCT05148715)

Calcineurin Inhibitor in NEuRoloGically Deceased Donors to Decrease Kidney delaYed Graft Function (CINERGY)-Pilot Trial

🔵 Active, Not Recruiting Phase2 💊 Investigational Drug / Biologic Sponsor: Université de Sherbrooke

🩺 Plain-English Summary (8th-Grade Level)

The investigators hypothesize that preconditioning neurologically deceased organ donors with the calcineurin inhibitor tacrolimus will improve short and long-term transplant survival without causing harm. Organ donors will be randomized to receive either 0.02 mg/kg ideal body weight (IBW) of tacrolimus single infusion or placebo before organ recovery. All corresponding recipients are enrolled and data is collected up to 7 days post-transplant to determine graft function and at 1 year to collect outcomes of vital status, re-transplantation and dialysis. The CINERGY Pilot Trial assesses feasibility for the main trial.

Who can join: Review the eligibility criteria below.

Location: Vancouver General Hospital — Vancouver, British Columbia

Age range: 18 Years to 100 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (9 Sites)

  • Vancouver General Hospital — Vancouver, British Columbia
  • St. Paul's Hospital — Vancouver, British Columbia
  • L'Institut de Cardiologie de Montréal — Montreal, Quebec
  • Hôpital Maisonneuve-Rosemont — Montreal, Quebec
  • Centre Hospitalier Universitaire de Montréal — Montreal, Quebec
  • Centre universitaire de santé McGill (CUSM) — Montreal, Quebec
  • Centre Hospitalier Universitaire de Québec- Université Laval — Québec, Quebec
  • Institut universitaire de cardiologie et de pneumologie de Québec (IUCPQ) — Québec, Quebec
  • Centre de recherche CHUS — Sherbrooke, Quebec

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗