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Search / Trial NCT04344613

Evaluation of the Clinical Performances of a Point of Care Analyzer Enabling Pre-transfusion ABOD Group Ultimate Verification at the Patient Bedside

Launched by FRANCIS CORAZZA · Apr 9, 2020

Trial Information

Current as of July 21, 2025

Unknown status

Keywords

ClinConnect Summary

ABO-incompatible red blood cell transfusions still represent an important hazard in transfusion medicine. Therefore, some countries have introduced a systematic bedside ABO agglutination test checking that the right blood is given to the right patient. However, this strategy is entirely manual, requires an extremely time-consuming learning program and relies on a subjective interpretation of agglutination on ABO test cards (for example Biorad, Diagast).

The ULB spinoff Antigon developed a prototype device on the basis of a technology developed in the Translational research laboratory of CH...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • For the device evaluation inside the laboratory : every patient for whom a blood group is ordered to the blood transfusion laboratory.
  • For the device bedside evaluation : each patient from the hematology unit (one day clinic) requiring a transfusion.
  • Exclusion Criteria:
  • Emergency circumstances requiring an urgent transfusion
  • Patient older than 80 years old
  • Patients with venous access

About Francis Corazza

Francis Corazza is a dedicated clinical trial sponsor committed to advancing medical research and innovation. With a focus on developing new therapeutic solutions, the organization collaborates with leading healthcare professionals and research institutions to design and implement rigorous clinical studies. Their approach emphasizes ethical practices, patient safety, and data integrity, ensuring that all trials adhere to the highest regulatory standards. Through a strategic commitment to transparency and collaboration, Francis Corazza aims to contribute significantly to the improvement of healthcare outcomes and the enhancement of patient quality of life.

Locations

Brussels, , Belgium

Patients applied

0 patients applied

Trial Officials

Hanane El Kenz, MD

Principal Investigator

CHU Brugmann

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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