Optimizing long-term prevention of cardiovascular disease after acute coronary syndrome

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study evaluates the effectiveness of a 'first-time-right' pharmacological treatment strategy for patients hospitalized with coronary artery disease. It compares this approach, which involves immediate initiation of a comprehensive medication plan, to the current practice of incremental titration of medications. The study aims to determine if the new strategy leads to a reduction in major adverse cardiovascular events over a 36-month period. Participants will be monitored through routine clinical visits and online questionnaires to assess outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* \>18 years of age (no upper limit)
* Coronary event, i.e. ACS or coronary revascularisation
* Able to provide informed consent

Exclusion Criteria:

* (short-term planned) pregnancy or breast feeding
* Dialysis

Where it's running

• Amsterdam UMC
  Amsterdam, Netherlands Recruiting

Study contacts

• Principal investigator: Harald T. Jorstad, dr. — Amsterdam UMC
• Study coordinator: Manon van den Bogaart, drs.
• Email: m.vandenbogaart@amsterdamumc.nl
• Phone: 003120 5660703

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.