Registry of patients treated with percutaneous coronary interventions at University of Fribourg
Percutaneous Coronary Intervention Registry FRIBOURG
This study tracks patients who receive stents for heart artery problems at the University of Fribourg to see how they do over time and improve treatment for everyone.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 3000 (estimated) |
| Ages | 17 Years to 120 Years |
| Sex | All |
| Sponsor | University of Freiburg Academic / other |
| Locations | 1 site (Fribourg) |
| Trial ID | NCT04185285 on ClinicalTrials.gov |
What this trial studies
This registry follows all consecutive patients who undergo percutaneous coronary interventions (PCI) at the University of Fribourg. The aim is to collect and analyze clinical data to improve understanding and outcomes related to coronary artery disease. Patients treated with stents will be monitored for their clinical progress and outcomes post-intervention. The observational nature of the registry allows for real-world data collection without altering standard treatment protocols.
Who should consider this trial
Good fit: Ideal candidates include all consecutive patients who are treated with PCI at the University of Fribourg and can provide informed consent.
Not a fit: Patients who are unwilling to participate or unable to provide informed consent will not benefit from this registry.
Why it matters
Potential benefit: If successful, this registry could enhance the understanding of PCI outcomes and improve treatment strategies for coronary artery disease.
How similar studies have performed: Similar registries have shown success in improving clinical outcomes and understanding of PCI, making this approach well-established.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All consecutive patients treated by percutaneous coronary intervention at our institution * Able to give informed consent and willing to participate Exclusion Criteria: * Unwillingness to participate * Enable to provide inform consent
Where this trial is running
Fribourg
- Cardiology, university Fribourg Medical Center — Fribourg, Switzerland (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.