Monitoring transfusions during anesthesia in emergency situations
Biological Transfusion Efficiency Registry Transfusion Surveillance in Anaesthesia
This study is looking at how blood transfusions are done during emergency surgeries to help improve future treatment guidelines for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50000 (estimated) |
| Sex | All |
| Sponsor | Erasme University Hospital Academic / other |
| Locations | 1 site (Anderlecht) |
| Trial ID | NCT06403163 on ClinicalTrials.gov |
What this trial studies
This observational study aims to collect comprehensive data on transfusion practices during active hemorrhage in patients undergoing anesthesia. By gathering detailed information from patient files, the study seeks to facilitate modeling and analysis related to emergency transfusion protocols. The data collection will occur without altering the patients' management and will be limited to the acute management period. Patients will be informed about their inclusion in the registry during their anesthesia consultation.
Who should consider this trial
Good fit: Ideal candidates for this study are patients who have received hemostatic products during anesthesia for active hemorrhage.
Not a fit: Patients who refuse to consent to data analysis and study participation will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the safety and effectiveness of transfusion practices in emergency situations.
How similar studies have performed: While similar studies on transfusion practices exist, this specific approach to monitoring during anesthesia in emergency situations is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * all patients who have received an hemostasis product Exclusion Criteria: * patient who refused to consent to data analysis and study participation
Where this trial is running
Anderlecht
- Université libre de Bruxelles — Anderlecht, Belgium (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.