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Clinical Trials in Spain / NCT07372170
Recruiting Observational

Observational Study to Evaluate the Effectiveness of DOACS for Secondary Thrombosis Prevention in Low-risk Thrombotic APS Patients

NCT07372170 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2025-12-01
Last updated
2026-01-30

Condition(s) studied

Antiphospholipid Syndrome (APS)Venous Thrombosis (Disorder)Thrombophilia

Study summary

This is an observational study designed to evaluate the effectiveness and safety of direct oral anticoagulants (DOACs) compared with vitamin K antagonists (VKAs) for the secondary prevention of thrombosis in patients with low-risk thrombotic antiphospholipid syndrome.

Antiphospholipid syndrome is an autoimmune disorder associated with an increased risk of thrombotic events. Although VKAs have traditionally been the standard treatment, DOACs are increasingly used in clinical practice in selected patients, despite limited evidence in this setting.

This study includes patients with previous venous thrombosis and a low-risk serological profile who are treated with either DOACs or VKAs according to routine clinical practice. The primary objective is to compare thrombotic recurrence and bleeding events between both treatment strategies.

The results of this study will contribute to improving knowledge about the use of DOACs in patients with low-risk thrombotic antiphospholipid syndrome.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (≥18 years) with a diagnosis of thrombotic antiphospholipid syndrome. * Low-risk antiphospholipid syndrome defined by previous venous thrombosis and a single or double positive antiphospholipid antibody profile (lupus anticoagulant, anticardiolipin antibodies, and/or anti-beta-2-glycoprotein I antibodies). * Patients receiving long-term anticoagulant treatment with direct oral anticoagulants or vitamin K antagonists according to routine clinical practice. * At least 2 weeks of continuous anticoagulant treatment before study inclusion. Exclusion Criteria: * Age \<18 years. * Triple antiphospholipid antibody positivity. * History of arterial thrombosis. * Anticoagulation for indications other than secondary prevention of venous thrombosis related to antiphospholipid syndrome.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Hospital Universitario Infanta Leonor Madrid Madrid Recruiting
Hospital Universitario Infanta Sofía Madrid Madrid Recruiting

More Infanta Leonor University Hospital trials in Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07372170 on ClinicalTrials.gov ↗ ← All trials in Spain