Registry for evaluating care in 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 aims to create a registry to evaluate the long-term clinical impact of diagnostics, treatments, and devices used for acute coronary syndrome (ACS). It addresses the limitations of randomized controlled trials (RCTs) by capturing real-world data on patient characteristics and treatment outcomes. The study will involve prospective registration of patients presenting with ACS, allowing for a comprehensive analysis of care quality and effectiveness in routine clinical practice. The use of electronic patient records will facilitate the collection of clinical parameters and outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* All patients presenting with ACS
* Age ≥ 18 years

Exclusion Criteria:

* No oral or signed informed consent available.

Where it's running

• Gelre Ziekenhuizem
  Apeldoorn, Gelderland, Netherlands Recruiting
• Rijnstate Arnhem
  Arnhem, Gelderland, Netherlands Recruiting
• Gelderse Vallei
  Ede, Gelderland, Netherlands Recruiting
• Ziekenhuis Rivierenland
  Tiel, Gelderland, Netherlands Recruiting

Study contacts

• Study coordinator: Dean R.P.P. Chan Pin Yin, MD
• Email: d.chanpinyin@antoniusziekenhuis.nl
• Phone: 088 - 320 12 28

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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.