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Principal Investigators

Thanks to all Participating Centers and collaborators for engaging in this research program!

Thanks to the CCCTG for endorsing this research project.

Thanks to the CNTRP for their precious contribution.

Pilot Study

Study Design:
A multi-center, prospective, observational study of 178 participants.

Setting:
Approximately 8 ICUs in Canada.

Sudy Population:
Deceased organ donors.

Study Intervention:
Data collection obtain by obsevation and review of hospital charts. Limited data are obtained throught relevant organ procurement organizations (OPOs).

Primary outcome:
Feasibility, based on:
1. Implementation of a waived consent model
2. Refinement of data collection procédures for adult intensive care units.
3. Development of efficient links to post-transplantation data.
4. Recipient data collection.

Secondary outcomes:
1. Pratice patterns
2. Knowledge translation
3. Quality assurance
4. Generic graft outcome
5. Therapy evaluation