The Effect of Retrograde Autologous Priming on Transfusion Requirements After Cardiac Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age10-110
SponsorPopulation Health Research Institute

About this trial

The TheRAPy vanguard trial is a multicentre, multiple period randomized, cluster crossover vanguard trial testing the feasibility of a full-scale trial to evaluate whether a centre-based policy of routine use of RAP versus a policy of crystalloid priming reduces RBC transfusion for patients undergoing cardiac surgery on cardiopulmonary bypass. It will also provide information about key parameters of the TheRAPy full-scale trial.

Eligibility criteria

Qualifiers

Hospitals completing >200 adult cardiac surgical cases a year; (ii) 95% of cardiovascular surgery group (i.e., cardiac anesthesiologists, surgeons, and perfusionists) agree to manage patients under both autologous priming policies as per their randomization schedule for the duration of the trial.

All patients undergoing cardiac surgery on cardiopulmonary bypass at an enrolled site during the trial period will be included in data collection.

Disqualifiers

Complete <=200 cardiac surgical cases.

<95% of their cardiovascular surgery group agrees to manage patients according to either of the two policies.

Trial design

Treatments tested in this trial

  • retrograde autologous priming (RAP)
  • Crystalloid priming

Treatment groups

4,500 Participants
are divided into 2 treatment groups