Clinical Trials Directory

Trials / Completed

CompletedNCT03114436

National Observational Study of Clinical Practices in Deceased Organ Donation

Canada-DONATE: National Observational Study of Clinical Practices in Deceased Organ Donation

Status
Completed
Phase
Study type
Observational
Enrollment
622 (actual)
Sponsor
McMaster University · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This is a 1-year national prospective cohort study that observes the medical management of consented deceased organ donors at hospitals across Canada with a high volume of deceased donation.

Detailed description

This prospective cohort study enrols consecutive adult deceased organ donors with a waiver of research consent and collects various data related to deceased donor care in the ICU from the time of consent for donation to the time of organ recovery. Clinical data includes donor characteristics, type of donation (after neurological death or cardiocirculatory death), resuscitation methods, cardiopulmonary monitoring techniques, medications, blood work, mechanical ventilation, diagnostic imaging, complications, and methods of death declaration. Various clinical data on deceased donors are collected prospectively from the time of consent for organ donation up to and including the day of organ recovery. The Canada-DONATE study is designed to develop a national platform for future clinical trials in deceased donor care. The main objectives include: 1. Establish specialized organ donation research teams at participating ICUs. 2. Observe, record, and describe ICU practices in deceased donor care (e.g., donor resuscitation, organ suitability assessments, death declaration) which are likely to vary by site, region and province and will be very important to inform clinical care protocols for future RCTs. 3. Engage and work with ODOs from each province to foster data sharing and develop procedures to enhance efficiency in future RCTs. 4. Investigate the comparative effectiveness of various ICU interventions in deceased donor care to improve the conversion of consented donors to actual donors and to improve the number of transplants per donor. 5. Produce specific knowledge translation tools that will serve in the future as clinical tools to enhance ICU care and research tools to facilitate RCTs.

Conditions

Interventions

TypeNameDescription
OTHERObservational Data CollectionAll aspects of deceased donor care in the ICU.

Timeline

Start date
2016-08-31
Primary completion
2018-07-31
Completion
2018-07-31
First posted
2017-04-14
Last updated
2019-05-23

Locations

29 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT03114436. Inclusion in this directory is not an endorsement.