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Study identifier: NCT03823547 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Future Optimal Research and Care Evaluation

Condition: Acute Coronary Syndrome · Myocardial Infarction  ·  Sponsor: J.M. ten Berg

PhaseN/A
Planned participants99999
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Rationale: Acute coronary syndrome (ACS) is the leading cause of death worldwide. To improve cardiovascular care, research is needed. Current guidelines are mainly based on well controlled RCT's, though evaluation of the impact of such RCT's in the real world is missing. In order to evaluate the impact and to overcome certain limitations of RCT's, a more practical approach is required. In this sense the use of nonrandomized observational studies is an important tool for determining the effectiveness of a therapy in routine clinical practice. One way to gain insight in characteristics of patients presenting in daily clinical practice, is to simply register these characteristics in a prospective manner with adequate follow up. Objective: To create an ongoing registry for evaluation of clinical long-term impact of diagnostics, various treatments and devices used for ACS, for research and evaluation of quality of care and to evaluate and improve regional quality of care and cooperation between PCI and non-PCI centers.

This description comes directly from the study's public registry record.

Talk to the study team

Dean R.P.P. Chan Pin Yin, MD  ·  088 - 320 12 28  ·  d.chanpinyin@antoniusziekenhuis.nl

Jur M. Ten Berg, MD, PhD  ·  088 - 320 13 82  ·  j.ten.berg@antoniusziekenhuis.nl

Always discuss trial participation with your own doctor first.

Locations (4)

Gelre ZiekenhuizemApeldoorn, Gelderland, NetherlandsRecruiting
Rijnstate ArnhemArnhem, Gelderland, NetherlandsRecruiting
Gelderse ValleiEde, Gelderland, NetherlandsRecruiting
Ziekenhuis RivierenlandTiel, Gelderland, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT03823547