Clinical Trials in France / NCT03479580
Recruiting
Observational
Coronary Artery Disease and Coronary Microvascular Disease in Cardiomyopathies Registry
NCT03479580 · tracked via the Priya Life Science France tracker
Condition(s) studied
HypertrophicIschemicRestrictive CardiomyopathyDilated Cardiomyopathies
Investigational drug(s) / intervention(s)
Patients with a cardiomyopathy
Patients with a cardiomyopathy: Prognostic value of coronary artery disease and microvascular disease in the different types of cardiomyopathies.
Study summary
Long-term prognostic value of macrovascular and microvascular coronary artery stenoses in each type of cardiomyopathy.
Eligibility
Inclusion Criteria:
* Ischemic
* Dilated
* Hypertrophic
* Restrictive cardiomyopathy.
Exclusion Criteria:
* Pregnant women
* Breastfeeding women
* Patients under legal protection
Primary outcome measure(s)
- Major Adverse Cardiovascular Events — 5 years
Composite outcome = rate of cardiovascular death, non-fatal myocardial infarction, need for myocardial revascularization by coronary artery bypass graft (CABG) or percutaneous coronary intervention (PCI) \> 3 months after enrollment. During follow up
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| University Hospital Grenoble | La Tronche | France | Recruiting |
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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 NCT03479580 on ClinicalTrials.gov ↗ ← All trials in France