Registry of patients who have had coronary artery procedures
Registry of Patients That Have Undergone an Invasive Coronary Angiography and/or Percutaneous Coronary Intervention
This study collects information from patients who have had heart procedures to better understand how these procedures relate to coronary artery disease.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Amsterdam UMC, location VUmc Academic / other |
| Locations | 1 site (Amsterdam) |
| Trial ID | NCT04815928 on ClinicalTrials.gov |
What this trial studies
This registry collects data from patients who have undergone invasive coronary angiography or percutaneous coronary intervention to assess the diagnostic and prognostic implications of various invasive measurements related to coronary artery disease. By analyzing these measurements, the study aims to enhance understanding of the functional significance of coronary artery disease. The observational nature of the study allows for real-world data collection without any specified interventions.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are undergoing clinically indicated invasive coronary angiography or percutaneous coronary intervention.
Not a fit: Patients who are not willing or unable to provide informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could improve the diagnostic and treatment strategies for patients with coronary artery disease.
How similar studies have performed: Other studies focusing on invasive measurements in coronary artery disease have shown promise, indicating that this approach is supported by prior research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years * Has undergone or will undergo a clinically indicated invasive coronary angiography. * Has undergone or will undergo a clinically indicated percutaneous coronary intervention. Exclusion Criteria: * Not willing / unable to provide informed consent.
Where this trial is running
Amsterdam
- Amsterdam Univeristy Medical centers, location VUmc — Amsterdam, Netherlands (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.