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NCT Number: NCT05995600

Comparison of Clopidogrel-based Antiplatelet Therapy Versus Warfarin As Secondary Prevention Strategy for AntiPhospholipid Syndrome-related STROKE

Antiphospholipid syndrome (APS) has a close association with ischemic stroke; however, the optimal treatment strategy for APS-related stroke has yet to be established. The clinical guidelines suggest using warfarin for APS-related stroke, but these suggestions are largely based on retrospective studies from the 1990s and expert opinion, rather than high-quality clinical trials. Moreover, the evidence on the role of antiplatelet drugs other than aspirin (e.g., clopidogrel) in APS-related stroke is particularly limited. Considering the relatively young age of patients with APS and the high clinical burden of using warfarin, it is necessary to verify whether warfarin is essential. Thus, the investigators aim to compare clopidogrel-based antiplatelet therapy and warfarin as a secondary preventive medication for patients with APS-related stroke. APS-STROKE is an exploratory, multicenter, prospective, randomized, open, blinded-endpoint clinical trial. Adult patients with definite APS who have a history of ischemic stroke will be included. Patients with high-risk APS (triple positivity or persistently high titers of anti-cardiolipin or anti-β2-glycoprotein I antibodies), systemic lupus erythematous, or indications for continued antiplatelet or anticoagulant therapy will be excluded. Eligible patients will be 1:1 randomized to receive clopidogrel-based antiplatelet therapy or warfarin. Patients assigned to the clopidogrel-based antiplatelet therapy group will be permitted to use additional antiplatelet drugs other than clopidogrel at the investigator's discretion. The primary outcome is a composite of any death, major adverse cardiovascular events, systemic thromboembolic events, and major bleeding during a follow-up period of at least 4 years. This study would provide valuable information for determining the optimal secondary prevention strategy for APS-related stroke.

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Hallym University Sacred Heart Hospital, Anyang, South Korea

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 19 years or older
  • History of ischemic stroke (cerebral infarction, transient ischemic attack, or retinal arterial ischemic event)
  • Patients who meet the laboratory diagnostic criteria for antiphospholipid syndrome (APS)
  • Patients or guardians who agree to the study protocol and sign with informed consent

Exclusion criteria

  • Patients with high-risk antiphospholipid antibody profile (triple positivity; persistent high-titers exceeding 80 U/mL of anti-cardiolipin or anti-β2 glycoprotein I antibodies)
  • Systemic lupus erythematous
  • Patients unable to discontinue previously taken anticoagulants or antiplatelet agents (e.g., atrial fibrillation, valvular heart disease, or a history of percutaneous coronary intervention)
  • Women who are pregnant, breastfeeding, or intending to become pregnant during the study period
  • Deemed unsuitable for participation in the study for more than four years, as per the investigators' discretion

Treatment and study plan

Antiplatelet Drug

Drug

Clopidogrel ± other antiplatelet drug

Warfarin

Drug

Warfarin (target prothrombin time-international normalized ratio 2.0-3.0)

Primary outcomes

  1. Composite endpoint

    Time frame: 4 years

    Composite endpoint of any death, major adverse cardiovascular events (MACEs), systemic thromboembolic events, and major bleeding. MACE includes any stroke, transient ischemic attack, and acute coronary syndrome (i.e., ST-elevation myocardial infarction, non-ST elevation myocardial infarction, and hospitalization with unstable angina) in this study. Major bleeding refers to bleeding events meeting the criteria for Bleeding Academic Research Consortium (BARC) type 3 or 5.

Secondary outcomes

  1. MACE

    Time frame: 4 years

    MACE includes any stroke, transient ischemic attack, and acute coronary syndrome (i.e., ST-elevation myocardial infarction, non-ST elevation myocardial infarction, and hospitalization with unstable angina) in this study.

  2. Ischemic stroke

    Time frame: 4 years

    Ischemic stroke or transient ischemic attack

  3. Any bleeding

    Time frame: 4 years

    Major or minor bleeding according to definitions from BARC

  4. Major bleeding

    Time frame: 4 years

    BARC bleeding type 3 or 5

  5. Intracranial bleeding

    Time frame: 4 years

    Intracranial bleeding that is objectively confirmed by brain imaging

  6. Clinically relevant non-major bleeding

    Time frame: 4 years

    Any bleeding that does not fit the criteria for major bleeding but does meet at least one of the following criteria:

    • requiring nonsurgical, medical intervention by a healthcare professional
    • leading to hospitalization or increased level of care
    • prompting evaluation.
  7. Any death

    Time frame: 4 years

    Death from any cause

  8. Thrombosis-related death

    Time frame: 4 years

    Death from arterial, venous, or capillary thrombotic events

Study contacts

Contact information is provided by the study sponsor or research team.

Seung-Hoon Lee, MD, PhD

CONTACT

[email protected]

+82-2-2072-1014

Wookjin Yang, MD, PhD

CONTACT

[email protected]

+82-2-2072-2114

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Collaborators

  • Samjin Pharmaceutical Co., Ltd.

Registry information

Official study title

Comparison of Clopidogrel-based Antiplatelet Therapy Versus Warfarin As Secondary Prevention Strategy for AntiPhospholipid Syndrome-related STROKE (APS-STROKE)

Acronym: APS-STROKE

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
Aug 16, 2023
Registry last updated
Oct 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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