Long-term anticoagulation for adults with severe hemophilia A

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational project will collect clinical data from adult patients with severe hemophilia A who receive long-term anticoagulation while on modern factor VIII prophylaxis, including extended half-life products. Researchers will document the type and dose of anticoagulant, details of FVIII replacement, bleeding and thrombotic events, and other clinical outcomes. No interventional treatment will be assigned — the work uses routine care and medical records, with inclusion dependent on absence of objection to data reuse. All cases are being gathered at the Hemostasis Unit, CHU de Strasbourg, creating a focused single-center case series to inform safety and management strategies.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adult patient (≥ 18 years) with severe hemophilia A
* Absence of written objection in the subject's medical record to the reuse of their data for scientific research purposes.

Exclusion Criteria:

\- Subject having expressed objection to the reuse of their data for scientific research

Where it's running

• Laboratoire d'Hématologie - Unité d'Hémostase - CHU de Strasbourg - France
  Strasbourg, France Recruiting

Study contacts

• Study coordinator: Laurent SATTLER, PharmD
• Email: laurent.sattler@chru-strasbourg.fr
• Phone: 33 3 88 12 75 28

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• SR604: a new treatment tested in adults with Hemophilia A/B or congenital Factor VII deficiency

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• NXT007 versus emicizumab to prevent bleeds in people with Hemophilia A

  This will test whether NXT007 prevents bleeding better than emicizumab in people aged 12 and older with Hemophilia A, including those with or without factor VIII inhibitors.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.