The effect of retrograde autologous priming on transfusion requirements after cardiac surgery [TheRAPy]: a multiple period vanguard cluster crossover trial – Australian arm (Trial Not Registered)

TheRAPy

This trial is Coming soon
Registration number Trial Not Registered
Significant blood dilution occurs during cardiac surgery involving cardiopulmonary bypass. One way to minimise this is a technique called retrograde autologous priming (RAP) whereby the patient’s own blood is used to prime the bypass circuit instead of a clear fluid solution. This study aims to assess the feasibility of a full-scale trial to determine if the routine use of RAP decreases the amount of blood transfused up to 72 hours post-surgery.

Program & service

This trial is being run with the Heart & Lung service, and as part of the Cardiothoracic Surgery program.

Trial phase

Pilot

Trial participation type

This trial is for clinical research of something other than a drug or device.

Principal investigator

A/Prof Tim Coulson

Key inclusion data

INCLUSION: Undergoing elective or urgent cardiac surgery requiring cardiopulmonary bypass (CPB) between 1 January 2027 and 31 December 2027. EXCLUSION: Routine RAP Policy: Patients deemed unsuitable for retrograde autologous priming (RAP) by the treating surgeon, anaesthetist, or perfusionist based on clinical assessment, these may include: Haemodynamic instability prior to CPB initiation/ Emergency initiation of CPB. Cardiogenic shock or requirement for preoperative mechanical circulatory support, including extracorporeal membrane oxygenation (ECMO), Impella®, or intra-aortic balloon pump (IABP).

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