Investigators are building an empirical evidence base for real world data through large-scale emulation of randomized controlled trials. The investigators' goal is to understand for what types of clinical questions real world data analyses can be conducted with confidence and how to implement such studies.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Major adverse cardiovascular events
Timeframe: 1 day after cohort entry date until the first of outcome or censoring, up to 365 days