NIH Registers Aspirin 50mg vs 100mg CVD Study NCT07542860
Summary
NIH's ClinicalTrials.gov has registered a new prospective cohort study (NCT07542860) evaluating 50mg versus 100mg daily aspirin for secondary prevention of atherosclerotic cardiovascular disease in approximately 5,448 Chinese patients aged 60 years and older, with follow-up extending to approximately 6 years through the LAPIS cohort extension.
What changed
NIH's ClinicalTrials.gov has registered NCT07542860, a prospective observational cohort study comparing 50mg versus 100mg daily aspirin in Chinese patients aged 60+ with atherosclerotic cardiovascular disease, extending the LAPIS cohort. The study will follow approximately 5,448 participants for an additional 2 years (total ~6 years) with primary outcomes assessing major adverse cardiovascular events and bleeding events. This registration provides researchers and healthcare providers information about an ongoing cardiovascular prevention study; it does not create compliance obligations for regulated entities.
Archived snapshot
Apr 21, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
Aspirin 50 mg vs. 100 mg in Elderly Cardiovascular Disease Patients
Observational NCT07542860 Kind: OBSERVATIONAL Apr 21, 2026
Abstract
Elderly patients with cardiovascular disease face a high risk of both thrombotic and bleeding events when receiving antithrombotic therapy. The optimal dose of aspirin for secondary prevention in this population remains uncertain, particularly in Chinese elderly individuals. This multicenter, prospective cohort study aims to evaluate the effectiveness and safety of a lower dose of aspirin (50 mg daily) compared with the standard dose (100 mg daily) for secondary prevention of atherosclerotic cardiovascular disease (ASCVD) in Chinese patients aged 60 years and older. The study is an extension of the existing LAPIS cohort (ChiCTR1900021980), which has enrolled 5,448 participants receiving long-term aspirin for secondary prevention. Participants will be followed for an additional 2 years (total follow-up up to approximately 6 years) through telephone, clinic visits, and electronic medical records. The primary effectiveness outcome is the first occurrence of major adverse cardiovascular events (MACE), including non-fatal myocardial infarction, unstable angina, need for revascularization, non-fatal stroke, transient ischemic attack, and cardiovascular death (excluding intracranial bleeding). The primary safety outcome is the first occurrence of bleeding events (classified by BARC criteria). A secondary aim is to develop and validate a risk prediction model (nomogram) for thrombotic and bleeding events specifically for elderly Chinese patients receiving antithrombotic therapy, u...
Conditions: Atherosclerotic Cardiovascular Disease (ASCVD), Secondary Prevention, Cardiovascular Diseases
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