Actively Recruiting
South East (Zuid Oost) Netherlands Heart Registry
Led by Radboud University Medical Center · Updated on 2024-07-25
99999
Participants Needed
4
Research Sites
1521 weeks
Total Duration
On this page
Sponsors
R
Radboud University Medical Center
Lead Sponsor
M
Maastricht Universitair Medisch Centrum
Collaborating Sponsor
AI-Summary
What this Trial Is About
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).
CONDITIONS
Official Title
South East (Zuid Oost) Netherlands Heart Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- No in- or exclusion criteria are applied to gain 100% registration in order to prevent bias.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
ZuyderlandMC
Heerlen, Limburg, Netherlands, 6419PC
Actively Recruiting
2
MaastrichtUMC+
Maastricht, Limburg, Netherlands, 6229 HX
Actively Recruiting
3
VieCuri
Venlo, Limburg, Netherlands, 5912 BL
Actively Recruiting
4
Radboud University Medical Centre
Nijmegen, Netherlands
Actively Recruiting
Research Team
V
van Geuns
CONTACT
V
Van 't Hof
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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