About this trial

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

Qualifiers

Patient receiving a comprehensive information about the study, and not opposed to participate

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 the possibility of follow-up of at least 6 months

Disqualifiers

Incomplete revised Sapporo-Sydney criteria

No data regarding the recurrent thrombosis

Pregnant woman

Age < 18 yo

Trial design

Treatments tested in this trial

  • Rivaroxaban

Treatment groups

No treatment groups listed

Locations

1
Stéphane Zuily54500, Nancy France

Sponsors and collaborators

Stéphane Zuily

Lead sponsor

Central Hospital, Nancy, France

Sponsor institution

International Society on Thrombosis and Haemostasis

Collaborator