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South East (Zuid Oost) Netherlands Heart Registry

South East (Zuid Oost) Netherlands Heart Registry (ZON-HR)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06512493
Acronym
ZON-HR
Enrollment
99999
Registered
2024-07-22
Start date
2020-11-01
Completion date
2050-01-01
Last updated
2024-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome, Chronic Coronary Syndrome, Coronary Artery Disease

Keywords

percutaneous coronary intervention, secondary prevention, chronic coronary syndrome, acute coronary syndrome, personalized medicine

Brief summary

Rationale: Patients undergoing percutaneous coronary intervention (PCI) for chronic coronary syndrome (CCS) or acute coronary syndrome (ACS) have a residual risk of ischemic events after PCI due to the progression of atherosclerosis in and outside the stented segments. The residual risk is affected by thrombotic, lipid, inflammation and diabetic risk factors. Secondary prevention after PCI is therefore of major importance to reduce complications and improve the patients' prognosis. Objective: To provide an extensive overview on the quality of secondary prevention and personalized medicine, a consortium in the South East Netherlands has created a PCI registry, the Zuid Oost Nederland Hart Registratie (ZON-HR).

Detailed description

Rationale: Patients undergoing percutaneous coronary intervention (PCI) for chronic coronary syndrome (CCS) or acute coronary syndrome (ACS) have a residual risk of ischemic events after PCI due to the progression of atherosclerosis in and outside the stented segments. The residual risk is affected by thrombotic, lipid, inflammation and diabetic risk factors. Secondary prevention after PCI is therefore of major importance to reduce complications and improve the patients' prognosis. Antithrombotic treatment plays a major role in the reduction of thromboembolic events and is therefore key in secondary prevention. However, this treatment increases the risk of bleeding complications. Therefore, a personalized antiplatelet strategy is recommended by the guidelines. Together with the antithrombotic treatment, lipid management is the cornerstone of secondary prevention. As low density lipoproteins cholesterol (LDL-C) increases the risk for atherosclerotic cardiovascular disease, the current ESC guidelines recommend a LDL-C value \<1.4mmol/L in patients undergoing PCI. Personalized medicine in which the treatment and lifestyle advice after PCI is adjusted on the patients' risk factors such as high bleeding- or thromboembolic risk, high LDL cholesterol levels, hypertension or the presence of diabetes mellitus (DM) is of major importance to lower the residual risk of complications and revascularisation. However, due to the large amount of risk factors that should be considered, personalized medicine is challenging which can lead to under treatment. Objective: To maintain and improve quality of care throughout the Netherlands, all interventional centres deliver data regarding patient- and procedural characteristics and follow-up after PCI to the Netherland Heart Registry (NHR). The NHR processes the data and provides these centres with feedback. (16) However, the registration of baseline-, procedural- and follow-up parameters by the NHR is concise and mainly focuses on mortality and (ischemia driven) revascularisation. To enhance the potency of this PCI registry, a consortium in the South East region of the Netherlands has created an extended version: The Zuid Oost Nederland Hart Registratie (ZON-HR). With this comprehensive registry, the ZON-HR provides a more extensive overview on the quality of secondary prevention and personalized medicine. Furthermore, the ZON-HR consortium aims to improve secondary prevention post-PCI by stimulating a personalized approach. Also, it will provide a platform for research regarding secondary prevention.

Interventions

None listed

Sponsors

Maastricht Universitair Medisch Centrum
CollaboratorUNKNOWN
Zuyderland Medisch Centrum
CollaboratorOTHER
VieCuri Medical Centre
CollaboratorOTHER
Radboud University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

No in- or

Exclusion criteria

are applied to gain 100% registration in order to prevent bias.

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with1 or 2 years* all- cause mortality * Myocardial infarction * Stent thrombosis * Stroke * Revascularisation * All bleeding events requiring medical evaluation

Countries

Netherlands

Contacts

Primary Contactvan Geuns
robertjan.vangeuns@radboudumc.nl(024) 3614153
Backup ContactVan 't Hof
arnoud.vant.hof@mumc.nl043 3872727

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026