Overview

PDE5i Use in Renal Transplant Recipients

Status:
Not yet recruiting
Trial end date:
2023-01-01
Target enrollment:
0
Participant gender:
All
Summary
Ischemia-reperfusion (IRI) injuries are common in renal transplantation and cause poor patient outcomes. Ischemia occurs after the donor's death and reperfusion occurs after kidney implantation. The donor kidney undergoes warm ischemia (WIT) after blood circulation stops and cold ischemia (CIT) when subjected to cold storage during transportation. Decreased blood flow leads to waste product accumulation and cellular damage. During reperfusion, reactive oxygen radicals and inflammatory processes further damage the kidney. PDE5 inhibitors increase renal blood flow and could protect the kidney during transplantation. Our study assesses the utility of giving these drugs perioperatively to reduce the effects of IRI injury.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of British Columbia
Treatments:
Sildenafil Citrate
Criteria
Inclusion Criteria:

- renal transplant patients at VGH undergoing donation after circulatory death (DCD) and
donation after brain death (DBD) kidney transplants

- 19 years of age

- able to provide consent.

Exclusion Criteria:

- Patients that are unable to understand the purpose of the study or cannot give written
consent will be excluded.

- Moreover, patients with contraindications to PDE5 inhibitors will be excluded from the
study. PDE5 inhibitors are generally well tolerated, even in patients with severe
renal disease, those on dialysis, and in transplant recipients. Patients will be
excluded if they are taking nitrates of any form (contraindication), are allergic to
sildenafil or any of the ingredients of this medication, are on an alpha-adrenergic
blocker (potential risk)

- patients currently on any experimental drug in the last 3 months (confounding factor).