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New study examines bleeding treatment in blood thinner patients

NCT ID NCT05898412

Knowledge-focused Sponsor: AstraZeneca Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at 217 Dutch patients who were hospitalized with serious bleeding while taking a type of blood thinner called a factor Xa inhibitor. All patients received a drug called andexanet alfa to reverse the bleeding. Researchers wanted to learn more about the patients' characteristics and what happened after treatment, including any blood clots. The study is based on past medical records from about 10 hospitals in the Netherlands.

What this could mean

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

Active substance
andexanet alfa
What this could lead to
If successful, this study could help doctors better understand which patients might benefit most from andexanet alfa and how to use it safely.
What could go wrong
This is a small, retrospective study that only looks back at past data. It cannot prove cause and effect, and results may not apply to all patients.

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

217 people

The number who actually took part.

Started

Oct 2023

Finished

Nov 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

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

Who is studied

Hospitalized patients \>18 years of age treated with at least one dose of andexanet alfa

Ages

18 years and older

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: * Age ≥ 18 years * Received at least one dose of andexanet alfa Exclusion Criteria: None

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Conditions

The condition(s) this trial relates to.

Hemorrhage

As listed by the trial registrant

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

Hemorrhage

Contacts and locations

Locations

  • Research Site

    Amsterdam, Netherlands

More trials for these conditions

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