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Massive study tracks blood transfusions to save lives in surgery

NCT ID NCT06403163

Knowledge-focused Sponsor: Erasme University Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This registry will collect detailed information from 50,000 patients who receive emergency blood transfusions during active bleeding while under anesthesia. The goal is to analyze how transfusions affect blood clotting, oxygen levels, and other vital signs. By studying this data, researchers hope to improve transfusion safety and outcomes for patients in critical situations.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this registry could help doctors better understand how to manage emergency transfusions and reduce complications.
What could go wrong
This is an observational registry, not a treatment trial. It collects data but does not test a new drug or therapy, so direct patient benefits may not be immediate.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 50,000 people

The number the study aims to enrol. It can still change while the study runs.

Started

Sep 2022

Expected to finish

Dec 2030

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

All patient who received an hemostasis product during an hemorrhagic situation

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * all patients who have received an hemostasis product Exclusion Criteria: * patient who refused to consent to data analysis and study participation

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Conditions

The condition(s) this trial relates to.

blood coagulation disease Emergencies Gastrointestinal Hemorrhage Hemorrhage Shock Transfusion Reaction

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Anesthesia Anesthesia; shock Blood coagulation disorder Blood loss Fresh blood stool Side effect Transfusion reaction Transfusion related complication

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Université libre de Bruxelles

    RECRUITING

    Anderlecht, 1070, Belgium

More trials for these conditions

Other studies related to the condition(s) this trial covers.