Condition: Acute Coronary Syndrome · Sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
The goal of this observational study is to evaluate the implementation of a 'first-time-right' pharmacological treatment strategy in patients hospitalized with coronary artery disease. The main question it aims to answer is: Does early (immediately post-event) initiation of a full set of guideline-based, individualized, preventive medication lead to reductions in cardiovascular events compared to current practice (incremental titration strategies)? Researchers will compare the 'first-time-right' strategy group to the current practice group to see if there are improvements in major adverse cardiac and cerebrovascular events (MACE) at 36 months. Participants will: * Receive either the 'first-time-right' strategy or current practice for secondary prevention. * Be monitored (data collection) through routine clinical visits at baseline, 8 weeks, 12, and additional telephone contacts at 24, and 36 months after discharge. * Complete online questionnaires at hospitalization, 8 weeks, 12, 24, and 36 months after discharge.
This description comes directly from the study's public registry record.
Manon van den Bogaart, drs. · 003120 5660703 · m.vandenbogaart@amsterdamumc.nl
Marjolein Snaterse, dr. · m.snaterse@amsterdamumc.nl
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| Amsterdam UMC | Amsterdam, Netherlands | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06637657