Antiplatelet Drug
DrugClopidogrel ± other antiplatelet drug
NCT Number: NCT05995600
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.
Interested in participating?
Request Info19 year and older
All sexes
Interventional
Phase 4
Hallym University Sacred Heart Hospital, Anyang, South Korea
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Clopidogrel ± other antiplatelet drug
Warfarin (target prothrombin time-international normalized ratio 2.0-3.0)
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.
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.
Time frame: 4 years
Ischemic stroke or transient ischemic attack
Time frame: 4 years
Major or minor bleeding according to definitions from BARC
Time frame: 4 years
BARC bleeding type 3 or 5
Time frame: 4 years
Intracranial bleeding that is objectively confirmed by brain imaging
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:
Time frame: 4 years
Death from any cause
Time frame: 4 years
Death from arterial, venous, or capillary thrombotic events
Contact information is provided by the study sponsor or research team.
Seung-Hoon Lee, MD, PhD
CONTACT
Wookjin Yang, MD, PhD
CONTACT
Seoul National University Hospital
Other
Comparison of Clopidogrel-based Antiplatelet Therapy Versus Warfarin As Secondary Prevention Strategy for AntiPhospholipid Syndrome-related STROKE (APS-STROKE)
Acronym: APS-STROKE
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.
Published trials that share one or more normalized conditions with this study.
NCT03684564
Antiphospholipid Syndrome, Autoimmune Diseases
Epsom, United Kingdom
View Trial DetailsNCT05195372
Antiphospholipid Syndrome, Arterial Thromboembolism
Frankfurt am Main, Hesse, Germany
View Trial DetailsNCT04262492
Anticoagulants Causing Adverse Effects in Therapeutic Use, Antiphospholipid Syndrome
Nancy, France
View Trial DetailsNCT07163338
Antiphospholipid Syndrome, Autoimmune Diseases
Reims, France
View Trial Details