International Registry of Thrombotic APS Patients Treated With Direct Oral Anticoagulants

Last updated: May 7, 2026
Sponsor: Stéphane Zuily
Overall Status: Active - Recruiting

Phase

N/A

Condition

Platelet Disorders

Antiphospholipid Syndrome

Thrombosis

Treatment

Rivaroxaban

Clinical Study ID

NCT04262492
2019-A01415-52
  • All Genders

Study Summary

This registry, currently being established will ensure consistency of data collection and provide safety information in non high-risk APS patients currently on DOACs.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patient receiving a comprehensive information about the study, and not opposed toparticipate

  • Age ≥ 18 yo

  • Classification of definite APS according to revised Sapporo-Sydney criteria

  • Direct oral anticoagulant treatment prescribed during at least 6 months or with thepossibility of follow-up of at least 6 months

Exclusion

Exclusion Criteria:

  • Incomplete revised Sapporo-Sydney criteria

  • No data regarding the recurrent thrombosis

  • Pregnant woman

  • Age < 18 yo

Study Design

Total Participants: 500
Treatment Group(s): 1
Primary Treatment: Rivaroxaban
Phase:
Study Start date:
October 21, 2020
Estimated Completion Date:
April 21, 2031

Connect with a study center

  • Stéphane Zuily

    Nancy, 54500
    France

    Active - Recruiting

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