Restrictive Transfusion StratEgy Adjusted by SvO2 During Cardiac Surgery (RETSEACSII)

January 14, 2026 updated by: University Hospital, Montpellier

Restrictive Transfusion StratEgy Adjusted by SvO2 During Cardiac Surgery: Multicenter, Single-blinded, Randomised Controlled Trial.

The goal of the clinical trial is to evaluate whether a restrictive transfusion strategy adjusted by SvO2 during the perioperative period of cardiac surgery may reduce the incidence of red blood cell transfusion. Adult patients operated on cardiac surgery will be randomly allocated into two groups, one receiving standard restrictive transfusion, the other receiving SvO2 adjusted restrictive transfusion.The proportion of patients transfused will be compared between the 2 groups.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Cardiac surgery represents only a small fraction of all surgical procedures, but consumes a significant proportion of the stored red blood cells (RBC), with almost 50% of patients receiving a perioperative transfusion. Since RBC transfusion is associated with an increased risk of morbidity and mortality, blood patient management strategy has been promoted to favour prevention of anaemia, reduction of bleeding and limitation of transfusion. Current guidelines recommend haemoglobin (Hb) threshold as low as 7 g/dL, but still with a wide possible range (7 to 9 g/dl) and suggest that Hb alone may not be the best criteria for triggering transfusion. As Hb is an oxygen carrier, the rationale for RBC transfusion should be to increase tissue oxygen delivery. Central venous oxygen saturation (central SvO2), which is related to the balance between tissue oxygen delivery and consumption, is easily measurable in cardiac surgery. In a previous study, the investigators showed that in anaemic patients having undergone cardiac surgery, restrictive transfusion according to central SvO2 allowed a significant reduction in RBC transfusion incidence in the ICU. The investigators hypothesize that a restrictive transfusion strategy adjusted by SvO2 during all the perioperative period of cardiac surgery may reduce further the incidence of RBC transfusion. Limiting RBC transfusion to patients with a low SvO2 could save unnecessary transfusions, without increasing the anaemia related risk.

Study Type

Interventional

Enrollment (Actual)

676

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Montpellier, France, 34295
        • Departement d'anesthésie et réanimation D - Arnaud de Villeneuve

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 85 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Aged above 18 years and under 85 years
  • Signed informed consent form from the patient or his/her close relative or surrogate (if present) before inclusion or when possible when the patient has been included in an emergency setting
  • Anaemic (Haemoglobin at inclusion ≤ 13 g/dL)
  • Operated on elective, on-pump cardiac surgery for : Coronary artery bypass graft (CABG); Aortic, mitral or tricuspid valve (replacement or repair); Ascending aorta;Left ventricle assistance device (LVAD)
  • Operated on urgent on-pump cardiac surgery for : CABG;Endocarditis;Aortic dissection; Heart transplantation
  • Subjects must be covered by public health insurance

Exclusion Criteria:

  • Patient with no central venous catheter inserted in the superior vena cava
  • Pregnant or breast feeding patient
  • Subject unable to read or/and write
  • Participation in another interventional clinical trial or administration of an unapproved drug within the last 4 weeks before the screening date
  • Medical history of heparin-induced thrombocytopenia contraindicating heparin use during surgery
  • Persons deprived of their liberty by a judicial or administrative decision, persons undergoing psychiatric care and persons admitted to a health or social establishment for purposes other than research

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Patients assigned to the Control group will be transfused if hemoglobin (Hb) concentration is lower than 9 g/d.
Active Comparator: Adjusted transfusion
Patients assigned to the SvO2 group will be transfused if Hb concentration is lower than 9 g/dL and central SvO2 ≤ 65%.
Patients assigned to the SvO2 group will be transfused if Hb concentration is lower than 9 g/dL and central SvO2 ≤ 65%. Transfusion will be repeated whenever Hb concentration is lower than 9 g/dL and central SvO2 ≤ 65% during surgery and in the ICU (until day 5). Central SvO2 will be measured on a blood sample obtained from the distal lumen of the central venous catheter. Oximetry will be used for measurement with a point-of-care of gas analysis.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
RBC transfusion incidence
Time Frame: During cardiac surgery and postoperative ICU stay up to postoperative day 5
Proportion of RBC transfused patients
During cardiac surgery and postoperative ICU stay up to postoperative day 5

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
RBC transfusion incidence during surgery
Time Frame: During cardiac surgery
Proportion of patients transfused with RBC during surgery
During cardiac surgery
RBC units transfused during surgery
Time Frame: During cardiac surgery
Number of RBC units transfused during surgery
During cardiac surgery
RBC transfusion incidence during postoperative ICU stay
Time Frame: During postoperative ICU stay
Proportions of patients transfused with RBC during postoperative ICU stay
During postoperative ICU stay
RBC units transfused during postoperative ICU stay
Time Frame: During postoperative ICU stay
Number of RBC units transfused during postoperative stay in ICU
During postoperative ICU stay
RBC transfusion incidence at hospital discharge or day 28
Time Frame: From cadiac surgery to hospital discharge or day 28
Proportions of patients transfused with RBC at hospital discharge or day 28
From cadiac surgery to hospital discharge or day 28
RBC units transfused at hospital discharge or day 28
Time Frame: From cardiac surgery to hospital discharge or day 28
Number of RBC units transfused at hospital discharge or day 28
From cardiac surgery to hospital discharge or day 28
Postoperative septic complications
Time Frame: From cardiac surgery to hospital discharge or day 28
Proportion of postoperative septic complications
From cardiac surgery to hospital discharge or day 28
Postoperative ischemic complications
Time Frame: From cardiac surgery to hospital discharge or day 28
Proportion of postoperative ischemic complications (myocardial infarction, stroke, mesenteric)
From cardiac surgery to hospital discharge or day 28
Postoperative acute kidney injury
Time Frame: From cardiac surgery to hospital discharge or day 28
Proportion postoperative AKI according to Kdigo stages
From cardiac surgery to hospital discharge or day 28
Postoperative liver dysfuncion
Time Frame: From cardiac surgery to hospital discharge or day 28
Proportion of postoperative increase in binirubin or plasma hepatic enzymes
From cardiac surgery to hospital discharge or day 28
Postoperative respiratory failure
Time Frame: From cardiac surgery to hospital discharge or day 28
Proportion of postoperative of Pa/Fi<200
From cardiac surgery to hospital discharge or day 28
Postoperative low cardiac output syndrome
Time Frame: From cardiac surgery to hospital discharge or day 28
Proportion of low cardiac output
From cardiac surgery to hospital discharge or day 28
Postoperative arythmias
Time Frame: From cardiac surgery to hospital discharge or day 28
Proportion of atrial fibrillation
From cardiac surgery to hospital discharge or day 28
Length of ICU stay
Time Frame: From ICU admission to ICU discharge ofr day 28
ICU length of stay (number of days)
From ICU admission to ICU discharge ofr day 28
Length of hospital stay
Time Frame: From ICU admission to hospital discharge or day 28
Hospital length of stay (number of days)
From ICU admission to hospital discharge or day 28
Postoperative anemia
Time Frame: From ICU admission to hospital discharge or day 28
Hemoglobin concentration
From ICU admission to hospital discharge or day 28
Death
Time Frame: From cardiac surgery to hospital discharge or day 28
Proportion of deaths
From cardiac surgery to hospital discharge or day 28
Effect of RBC transfusion on Hb
Time Frame: During cardiac surgery and postoperative ICU stay up to postoperative day 5
Hb changes after RBC transfusion
During cardiac surgery and postoperative ICU stay up to postoperative day 5
Effect of RBC transfusion on central SvO2
Time Frame: During cardiac surgery and postoperative ICU stay up to postoperative day 5
Central SvO2 changes after RBC transfusion
During cardiac surgery and postoperative ICU stay up to postoperative day 5

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Pascal COLSON, MD, University Hospital, Montpellier

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 14, 2023

Primary Completion (Actual)

October 15, 2025

Study Completion (Actual)

October 21, 2025

Study Registration Dates

First Submitted

February 6, 2023

First Submitted That Met QC Criteria

February 21, 2023

First Posted (Actual)

February 22, 2023

Study Record Updates

Last Update Posted (Estimated)

January 16, 2026

Last Update Submitted That Met QC Criteria

January 14, 2026

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • RECHMPL21_0529

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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