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Clinical Trials in the Netherlands / NCT07773272
Recruiting Observational

Cardiovascular-kidney-metabolic (CKM)-Guided Therapy for Patients After Acute Coronary Syndrome

NCT07773272 · tracked via the Priya Life Science Netherlands tracker
Phase
Observational
Started
2026-03-16
Last updated
2026-08-19

Condition(s) studied

Acute Coronary Syndrome (ACS) Undergoing Percutaneous Coronary Intervention (PCI)HypercholerolemiaHypertensionDiabete MellitusCardiovascular Risk Management

Investigational drug(s) / intervention(s)

Rapid ESC-guideline based secondary prevention following myocardial infaction

Rapid ESC-guideline based secondary prevention following myocardial infaction: In the intervention group, patients will be treated according to a rapid ESC-guideline-based protocol. This approach will target: 1\. Optimal pharmacological treatment, including: * Lipid-lowering * Antihypertensive * Diabetic, such sodium-glucose co-transporter 2 inhibitors (SGLT-2 inhibitors) * Glucagon-like peptide-1 agonists (GLP-1 agonists)

Study summary

Patients with a history of myocardial infarction are at significantly increased risk of recurrent cardiovascular events. Despite established clinical guidelines, secondary preventive care is often initiated too late, inadequate in intensity or incomplete in application. As a result, important opportunities to prevent serious outcomes are missed.

The aim of this project is to investigate whether rapid, guideline-based treatment following myocardial infarction leads to improved patient outcomes. The study protocol is based on current clinical guidelines and targets key domains including diabetes, hypertension, and hypercholesterolemia. Outcomes of patients treated according to the study protocol will be compared to those receiving standard care. Primary endpoints include major adverse cardiac- and cerebrovascular events within a 24-month follow-up period.

The investigators hypothesize that rapid, guideline-based intervention will result in improved risk factor management, leading to a reduction in cardiovascular events and mortality. For patients, this may translate into improved health, quality of life and life expectancy. This project aims to deliver a practical protocol for effective secondary prevention in clinical practice, which is expected to reduce healthcare utilization in the long term. With this initiative, the investigators seek to take a significant step toward improving post-myocardial infarction care and contributing to sustainable cardiovascular healthcare.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age \> 18 years * Hospitalised with acute coronary syndrome * Underwent percutaneous coronary intervention Exclusion Criteria: * Acute coronary syndrome secondary to other diseases * Life expectancy \< 1 year based on the clinician's expertise

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Cardiology Heerlen Limburg Recruiting

More Zuyderland Medisch Centrum trials in the Netherlands

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07773272 on ClinicalTrials.gov ↗ ← All trials in the Netherlands