New global registry tracks safety of common blood thinners in APS patients

NCT ID NCT04262492

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study is creating a global registry of 500 adults with antiphospholipid syndrome (APS) who are taking direct oral anticoagulants (DOACs) like rivaroxaban or apixaban. Researchers will track rates of recurrent blood clots and bleeding over at least 6 months. The goal is to gather real-world safety information for this specific patient group.

What this could mean

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

Active substance
Direct oral anticoagulants (rivaroxaban, dabigatran, apixaban, edoxaban)
What this could lead to
If successful, this registry could provide clearer safety data on using DOACs in low-risk APS patients, potentially guiding future treatment decisions.
What could go wrong
This is an observational registry, not a controlled trial, so it cannot prove cause and effect. Results may be limited by patient selection and real-world variability.

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

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for ANTICOAGULANTS CAUSING ADVERSE EFFECTS IN THERAPEUTIC USE are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Stéphane Zuily

    RECRUITING

    Nancy, 54500, France

More trials for these conditions

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