Monitoring transfusions during anesthesia in emergency situations

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* all patients who have received an hemostasis product

Exclusion Criteria:

* patient who refused to consent to data analysis and study participation

Where it's running

• Université libre de Bruxelles
  Anderlecht, Belgium Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.