International Registry of Thrombotic APS Patients Treated With Direct Oral Anticoagulants

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorStéphane Zuily

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

Sponsors and collaborators

Stéphane Zuily

Lead sponsor

Central Hospital, Nancy, France

Sponsor institution

International Society on Thrombosis and Haemostasis

Collaborator