Health TrialsbyHealthPanel

Transfusion Surveillance in Anaesthesia

ConditionsTransfusion ReactionTransfusion Related ComplicationAnesthesiaAnesthesia; ShockSide EffectFresh Blood StoolBlood Coagulation DisorderBlood Loss
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorErasme University Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

all patients who have received an hemostasis product

Disqualifiers

patient who refused to consent to data analysis and study participation

Trial population

All patient who received an hemostasis product during an hemorrhagic situation

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Transfusion

    Procedure/Surgery

    Transfusion of an hemostatic product

Treatment groups

50,000 Participants
are divided into 1 treatment group
Group A: Transfused patients1 intervention

Trial outcomes

Primary outcomes

1

Hemostatic evolution through transfusion event

evolution of APTT (seconds)

Time frame
12 hours
2

ROTEM measures evolution through transfusion event

evolution of APTEMCT (seconds)

Time frame
12 hours
3

Haematologic measures evolution through transfusion event

evolution of hemoglobin (g/dL)

Time frame
12 hours
4

ionic measures evolution through transfusion event

evolution of lactate (mmol/L)

Time frame
12 hours

Secondary outcomes

1

Mortality at one month

Mortality at one month

Time frame
one month

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Erasme University Hospital

Lead sponsor

Source ClinicalTrials.gov
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