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Trial intelligence / Profile preview
NCT05283356Phase 4
Key facts
Phase 4, randomised trial of ticagrelor in aortic valve stenosis (2 arms), sponsored by Fundación Biomédica Galicia Sur. Primary endpoint: Net Adverse Clinical Events at 12 months. Started Jan 2022; status: recruiting.
Aspirin 100mg/day
Acetylsalicylic acid 100mg/day after TAVI
Ticagrelor 60mg BID
Ticagrelor 60 mg twice per day after TAVI
Adults with severe symptomatic aortic stenosis accepted for TAVI, with at least one comorbidity (diabetes, CAD, or PAD). Excludes patients requiring chronic oral anticoagulation, with recent ischemic stroke, severe hepatic insufficiency, or active bleeding.
Net Adverse Clinical Events
Subclinical valve thrombosis
Major bleeding
Patient-oriented composite endpoints
Beyond the preview
Full results, competitive context and analysis are in the Gosset platform.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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