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Transfusion Surveillance in Anaesthesia

Biological Transfusion Efficiency Registry Transfusion Surveillance in Anaesthesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06403163
Acronym
STAR
Enrollment
50000
Registered
2024-05-07
Start date
2022-09-01
Completion date
2030-12-31
Last updated
2025-09-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Keywords

transfusion, monitoring, emergency situation, shock, fresh frozen plasma

Brief summary

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.

Detailed 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.

Interventions

PROCEDURETransfusion

Transfusion of an hemostatic product

Sponsors

Erasme University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* all patients who have received an hemostasis product

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Hemostatic evolution through transfusion event12 hoursevolution of APTT (seconds)
ROTEM measures evolution through transfusion event12 hoursevolution of APTEMCT (seconds)
Haematologic measures evolution through transfusion event12 hoursevolution of hemoglobin (g/dL)
ionic measures evolution through transfusion event12 hoursevolution of lactate (mmol/L)

Secondary

MeasureTime frameDescription
Mortality at one monthone monthMortality at one month

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026