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Clinical Trials in Canada / NCT07698262
Starting soon Observational

Brain-based Prediction of the Dying Duration in Humans After Withdrawal of Life Sustaining Therapies to Inform Donation After Circulatory Death

NCT07698262 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2027-01
Last updated
2026-08-21

Condition(s) studied

Organ Donation After Circulatory Death

Study summary

The purpose of this study is to develop a new tool that uses information collected before life-sustaining treatments are withdrawn to better predict whether a patient will die within the time needed for organ donation to be possible. The tool created should help improve planning for organ donation and provide families and healthcare teams with more accurate information.

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥ 19; 2. Eligible for DCD Exclusion Criteria: 1. Complete high cervical spinal cord injury (C5 and above) 2. Pacemaker in situ 3. Tracheostomy

Primary outcome measure(s)

Trial sites (11)

FacilityCityRegionStatus
Cumming School of Medicine Calgary Alberta
UBC/East Kootenay Regional Hospital Cranbrook British Columbia
Kelowna General Hospital Kelowna British Columbia
Royal Columbian Hospital New Westminster British Columbia
Surrey Memorial Hospital Surrey British Columbia
Vancouver General Hospital Vancouver British Columbia
University of Manitoba Health Sciences Center Winnipeg Manitoba
University Hospital - London Health Sciences Centre London Ontario
Lakeridge Health Oshawa Ontario
Children's Hospital of Eastern Ontario (CHEO) Ottawa Ontario
St Paul hospital Vancouver Canada

More University of British Columbia trials in Canada

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 NCT07698262 on ClinicalTrials.gov ↗ ← All trials in Canada