Actively Recruiting
Biological Transfusion Efficiency Registry Transfusion Surveillance in Anaesthesia
Led by Erasme University Hospital · Updated on 2025-09-02
50000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research collects detailed information about blood transfusions given during active bleeding in patients undergoing anesthesia. The goal is to gather comprehensive data to support modeling and analysis related to emergency transfusion situations. The study is observational and does not change patient care during the process. Participants include patients who receive a transfusion of hemostatic products to manage bleeding. Data collection happens through reviews of patient medical records by investigators at the treatment center. This process only covers the acute management period and does not involve any experimental treatments. During the study, researchers will monitor changes in blood clotting, hematologic values, and ionic measures over 12 hours following the transfusion event. They will also track mortality rates at one month. Patients will be informed about their inclusion during anesthesia consultations, and all data are collected without altering their treatment.
CONDITIONS
Brief Title
Transfusion Surveillance in Anaesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients who have received a hemostasis product
You will not qualify if you...
- Patients who refused to consent to data analysis and study participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - Up to the time of anesthesia consultation
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) during anesthesia consultation
Duration - Up to 12 hours during acute transfusion management
Participants who undergo routine care are observed during the acute management of the transfusion event. Data related to transfusion and biological measures are collected without modifying participant management.
Data collected from patient files during routine care
Duration - Up to one month after transfusion
Participants are monitored for outcomes such as mortality following the transfusion event.
Follow-up data collected from medical records
Trial Site Locations
Total: 1 location
1
Université libre de Bruxelles
Anderlecht, Belgium, 1070
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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