Trial of Indication-Based Transfusion of Red Blood Cells in ECMO

Last updated: March 24, 2025
Sponsor: Boston Children's Hospital
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

Red blood cell transfusion

Clinical Study ID

NCT05405426
W81XWH-22-1-0301
  • Ages < 6
  • All Genders

Study Summary

TITRE - Trial of Indication-based Transfusion of Red Blood Cells in ECMO, is a multicenter, prospective, randomized clinical trial. The overarching goal of TITRE is to determine whether restricting red blood cell (RBC) transfusion according to an indication-based strategy for those with bleeding and/or deficit of tissue oxygen delivery, compared with transfusion based on center-specific hemoglobin or hematocrit thresholds, can reduce organ dysfunction and improve later neurodevelopment in critically ill children receiving Extracorporeal Membrane Oxygenation (ECMO) support.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Age < 6 year at ECMO cannulation

  2. Veno-arterial (VA) mode of ECMO

  3. First ECMO run during the index hospitalization

Exclusion

Exclusion Criteria:

  1. Gestationally-corrected age < 37 weeks at the time of ECMO cannulation

  2. Veno-venous (VV) mode of ECMO

  3. Patients initially started on VV-ECMO and then transitioned to VA ECMO > 18 hoursafter ECMO cannulation

  4. ECMO used for procedural support (ECMO deployed and decannulated in procedural areawith no ICU ECMO care) or ECMO duration expected to be < 24 h

  5. Limitation of care in place or being discussed

  6. Congenital bleeding disorders

  7. Hemoglobinopathies

  8. Primary Residence outside country of enrollment

  9. Concurrent participation in a separate interventional trial that has potential toimpact neurodevelopment status of patient. (note that observationalnon-interventional studies do not qualify the patient for exclusion). This includesa patient already enrolled in TITRE

  10. Lack of access to medical records required for calculation of pre-ECMO pSOFA scoredue to cannulation for ECMO at a non-trial center.

  11. Randomization not possible within 36 h following ECMO cannulation (e.g., due tostaffing or delays related to communication with participant family)

  12. Planned transition to ventricular assist device (VAD) within 48 hours of commencingECMO.

  13. Clinically documented indication for a Red Blood Cell transfusion threshold thatdiffers from the center-specific transfusion threshold (e.g., oncological treatmentthat limits donor exposure).

Study Design

Total Participants: 228
Treatment Group(s): 1
Primary Treatment: Red blood cell transfusion
Phase:
Study Start date:
April 14, 2023
Estimated Completion Date:
October 31, 2026

Study Description

Observational studies of children on ECMO have shown an association between large-volume RBC transfusion and mortality. However, the hematocrit (or hemoglobin) level at which optimal tissue oxygen delivery occurs is unknown. TITRE - Trial of Indication-based Transfusion of Red Blood Cells in ECMO, is a prospective, randomized clinical trial to be conducted at 18-20 study sites. The overarching goal of TITRE is to determine whether restricting RBC transfusion according to an indication-based strategy for those with bleeding and/or deficit of tissue oxygen delivery, compared with transfusion based on center-specific hemoglobin or hematocrit thresholds, can reduce organ dysfunction and improve later neurodevelopment in critically ill children receiving ECMO support.

Aim 1: To test whether children < 6 years of age on ECMO support who are randomized to a strategy of indication-based versus center-specific threshold-based RBC transfusion will have greater improvement in organ function.

Aim 2: To test whether survivors among children age < 6 years on ECMO support who are randomized to indication-based compared to center-specific threshold-based RBC transfusion will have better neurodevelopmental outcomes and health-related QOL at one year post-randomization.

Key design features include: Randomization stratified by patient age (neonate:

=< 28d vs. non-neonate) and by diagnosis (CHD vs. other diagnosis); and a target sample size of 228 patients. Endpoints will be evaluated during ECMO, at hospital discharge, and at 3, 6, 9, and 12 months. To ensure trial integrity, the primary outcome (pSOFA: Pediatric Sequential Organ Failure Assessment score) will be adjudicated by an independent committee and neurodevelopmental assessments will be blinded.

Connect with a study center

  • The Children's Hospital at Westmead

    Westmead, New South Wales
    Australia

    Active - Recruiting

  • The Hospital for Sick Children

    Toronto, Ontario M5G 1X8
    Canada

    Active - Recruiting

  • Phoenix Children's Hospital

    Phoenix, Arizona 85016
    United States

    Active - Recruiting

  • Arkansas Children's Hospital

    Little Rock, Arkansas 72202
    United States

    Active - Recruiting

  • Children's Hospital Los Angeles

    Los Angeles, California 90027
    United States

    Active - Recruiting

  • Lucile Packard Children's Hospital

    Palo Alto, California 94304
    United States

    Active - Recruiting

  • Children's Hospital Colorado

    Aurora, Colorado 80045
    United States

    Active - Recruiting

  • Children's Healthcare of Atlanta

    Atlanta, Georgia 30322
    United States

    Active - Recruiting

  • Lurie Children's Hospital

    Chicago, Illinois 60611
    United States

    Active - Recruiting

  • Riley Children's Hospital

    Indianapolis, Indiana 46202
    United States

    Active - Recruiting

  • Boston Children's Hospital

    Boston, Massachusetts 02115
    United States

    Active - Recruiting

  • University of Michigan Medical Center

    Ann Arbor, Michigan 48109
    United States

    Active - Recruiting

  • Children's Hospital of Michigan

    Detroit, Michigan 48201
    United States

    Active - Recruiting

  • Washington University in St. Louis School of Medicine

    Saint Louis, Missouri 63110
    United States

    Site Not Available

  • Duke University Hospital

    Durham, North Carolina 27710
    United States

    Site Not Available

  • Cincinnati Children's Hospital Medical Center

    Cincinnati, Ohio 45229
    United States

    Active - Recruiting

  • Children's Hospital of Philadelphia

    Philadelphia, Pennsylvania 19104
    United States

    Active - Recruiting

  • MUSC Shawn Jenkins Children's Hospital

    Charleston, South Carolina 29425
    United States

    Active - Recruiting

  • Monroe Carell Jr. Children's Hospital at Vanderbilt

    Nashville, Tennessee 37232
    United States

    Active - Recruiting

  • Children's Health Dallas University of Texas Southwestern

    Dallas, Texas 75235
    United States

    Active - Recruiting

  • Texas Children's Hospital - Baylor College of Medicine

    Houston, Texas 77030
    United States

    Active - Recruiting

  • Primary Children's Hospital

    Salt Lake City, Utah 84132
    United States

    Active - Recruiting

  • Inova Children's Hospital

    Falls Church, Virginia 22042
    United States

    Active - Recruiting

  • Seattle Children's Hospital

    Seattle, Washington 98105
    United States

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.