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Completed

NCT Number: NCT01484639

Transfusion Requirements in Cardiac Surgery

This is a multi-centre randomized controlled pilot trial of two transfusion strategies in high risk patients having cardiac surgery. This study will be conducted in 7 Canadian centers and 1 American centre. Patients allocated to a "restrictive" transfusion strategy will receive a red cell transfusion if their hemoglobin is 75 g/L or less intraoperatively and postoperatively. Patients allocated to a "liberal" transfusion strategy will receive red cell transfusion if their hemoglobin concentration is 95 g/L or less intraoperatively and postoperatively in the intensive care unit, and less than 85 g/L on the ward.

The primary objectives of this study are to determine 1) enrollment rates (patients enrolled/patients eligible), 2) consent rates (consent obtained/patients approached); and 3) protocol adherence (incidence and reasons for non adherence, lack of consent, rates of contamination and utilization of co-interventions). The secondary objectives are to determine 1) the mortality rate and the rate of the composite outcome for morbidity of renal, cardiac, neurological and infectious adverse events; 2) the proportion of missing data as a measure of the feasibility of the case report form; and 3) the proportion of blood products utilized (red cells, platelets and plasma).

The results of the multicentre pilot study will be used to 1) maximize enrollment rates to ensure timely completion of recruitment of a definitive large randomized controlled trial, 2) maximize adherence rates, 3) determine event rates for sample size estimation for a definitive study, and to 4) optimize the case report form.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Foothills Medical Centre, Calgary, Alberta, Canada

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years or older
  • European System for Cardiac Operative Risk Evaluation (EuroSCORE) of 6 or more
  • Consent

Exclusion criteria

  • Pregnancy
  • Refusal of blood products
  • Participating in autologous blood donation program
  • Based on the preoperative hemoglobin, the predicted hematocrit on cardiopulmonary bypass is greater than 33% (hemoglobin concentration of 110 g/L) or less than 18% (hemoglobin concentration of 60 g/L)

Treatment and study plan

Liberal transfusion triggers

Other

Patients allocated to a "liberal" transfusion strategy will receive red cell transfusion if their hemoglobin concentration is 95 g/L or less intraoperatively and postoperatively in the intensive care unit, and less than 85 g/L on the ward.

Restrictive transfusion triggers

Other

Patients allocated to a "restrictive" transfusion group will receive a red cell transfusion if their hemoglobin is 75 g/L or less intraoperatively and postoperatively.

Primary outcomes

  1. Enrollment rate

    Time frame: baseline

    To determine enrollment rates (patients enrolled/patients eligible), consent rates (consent obtained/patients approached)

  2. Protocol adherence

    Time frame: 28 days or hospital discharge

    To determine protocol adherence (incidence and reasons for non adherence, lack of consent, rates of contamination and utilization of co-interventions).

Secondary outcomes

  1. Mortality and morbidity

    Time frame: 28 days or hospital discharge

    To determine the mortality rate and a composite outcome for morbidity (renal, cardiac, neurological and infectious adverse events).

  2. Missing data

    Time frame: 28 days or hospital discharge

    To determine the proportion of missing data as a measure of the feasibility of the case report form

  3. Blood product utilization

    Time frame: 28 days or hospital discharge

    To determine the proportion of blood products utilized (red cells, platelets and plasma)

Sponsors and collaborators

Lead sponsor

Nadine Shehata

Other

Collaborators

  • Canadian Institutes of Health Research (CIHR)
  • Health Canada

Registry information

Official study title

Transfusion Requirements in Cardiac Surgery (TRICS II): A Randomized Controlled Trial

Acronym: TRICSII

Important dates

Study start
2012
Primary completion
2012
Study completion
2012
First posted
Dec 2, 2011
Registry last updated
Feb 21, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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