ClinConnect ClinConnect Logo
Search / Trial NCT06840756

Effects of Donor-recipient Sex-matched Blood Transfusion on Patient Outcomes

Launched by MICHELLE ZELLER · Feb 19, 2025

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Transfusions Red Blood Cell Transfusions Sex Matched Sex Mismatched Intensive Care Unit Icu Cardiovascular Circulatory Hematology Mortality Blood Donor Characteristics

ClinConnect Summary

This clinical trial is looking at how the sex of blood donors may affect how well patients do after receiving red blood cell (RBC) transfusions. Currently, blood transfusions are mostly based on matching blood types, without considering whether the donor and recipient are the same sex. Some research suggests that matching the donor's sex to the recipient's could improve patient outcomes. In this study, adult patients in the Intensive Care Unit (ICU) who need a blood transfusion will be randomly assigned to receive either sex-matched or sex-mismatched RBCs. The goal is to see if there are differences in survival rates between the two groups.

To be eligible for this trial, participants must be adults aged 18 or older, currently admitted to a participating ICU, and require an RBC transfusion. However, those with rare blood types or who are experiencing severe bleeding won't be included. If you or a loved one meets the criteria, you can expect to be part of a study that could help improve future blood transfusion practices and potentially save lives. The trial is not yet recruiting participants, but it aims to gather important information that could change how blood transfusions are ordered and managed in hospitals.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Adults (age ≥18);
  • Admission to a participating ICU;
  • Requiring RBC transfusion.
  • Exclusion Criteria:
  • Requirement for a specialized RBC product or unit not readily available in inventory (e.g., rare blood type, washed RBCs, complex RBC antibodies, etc.);
  • Massively bleeding patient (i.e., ≥4 units of blood ordered at one time, or Massive Hemorrhage Protocol initiated, or an urgent blood request made);
  • Sex unknown or sex other than male or female (i.e. intersex);
  • Do not have a valid Ontario Health Insurance Plan (OHIP) health card number.

About Michelle Zeller

Michelle Zeller is an experienced clinical trial sponsor dedicated to advancing medical research through innovative study designs and rigorous oversight. With a strong background in clinical operations and regulatory compliance, she leads initiatives that aim to enhance patient outcomes and contribute to the development of cutting-edge therapies. Committed to collaboration and ethical practices, Zeller fosters partnerships with research institutions and healthcare professionals to ensure the highest standards of trial execution. Her focus on data integrity and patient safety underscores her leadership in the clinical trial landscape.

Locations

Toronto, Ontario, Canada

Toronto, Ontario, Canada

Toronto, Ontario, Canada

Hamilton, Ontario, Canada

Kingston, Ontario, Canada

London, Ontario, Canada

Oshawa, Ontario, Canada

Ottawa, Ontario, Canada

Patients applied

0 patients applied

Trial Officials

Michelle Zeller, Doctor of Medicine

Principal Investigator

McMaster University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported