Transfusion Surveillance in Anaesthesia (STAR)

Free University of Brussels (ULB)

Status: Enrolling

Conditions: Transfusion Reaction; Fresh Blood Stool; Transfusion Related Complication; Side Effect; Blood Loss; Anesthesia; Shock; Blood Coagulation Disorder; Anesthesia

Treatments: Procedure: Transfusion

Study type: Observational

Funder types: Other

Identifiers

NCT06403163

STAR

Details and patient eligibility

About

the aim of this register is to collect exhaustively the different data available surrounding a transfusion act in the context of an active haemorrhage. The aim is to allow different modelling and analysis related to emergency transfusion.

Full description

the aim of this register is to collect exhaustively the different data available surrounding a transfusion act in the context of an active haemorrhage. The aim is to allow different modelling and analysis related to emergency transfusion.

Patients will be informed at the time of the anaesthesia consultation about the inclusion in the registry.

The data will be collected from the patients' files by the investigators of the centre without modifying their management.

The data collection period will not exceed the period of acute management.

Enrollment: 50,000 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• all patients who have received an hemostasis product

Exclusion criteria

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

Trial design

50,000 participants in 1 patient group

Transfused patients

Description:

patients who received an hemostatic product

Treatment:

Procedure: Transfusion