Registry of patients treated with percutaneous coronary interventions at University of Fribourg
Official title: Percutaneous Coronary Intervention Registry FRIBOURG
Run by University of Freiburg · NCT04185285 · Data updated 2026-11-12
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 |
|---|---|
| Ages | 17 Years to 120 Years |
| Sex | All |
| Enrollment | 3000 (estimated) |
| Sponsor | University of Freiburg Academic / other |
| Locations | 1 site (Fribourg) |
| Status | Recruiting |
| Started | May 1, 2015 |
| Main results expected | September 1, 2017 |
| Study ends | September 1, 2027 |
| Registry record updated | October 22, 2021 |
| Trial ID | NCT04185285 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include all consecutive patients who are treated with PCI at the University of Fribourg and can provide informed consent.
✕Probably not a fit
Patients who are unwilling to participate or unable to provide informed consent will not benefit from this registry.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
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 gone: Similar registries have shown success in improving clinical outcomes and understanding of PCI, making this approach well-established.
Who can join: the full rules
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 it's running
-
Cardiology, university Fribourg Medical Center
Fribourg, Switzerland Recruiting
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Aspirin 50 mg vs 100 mg with a P2Y12 inhibitor after PCI
This trial tests whether a 50 mg daily aspirin dose, when used with a P2Y12 inhibitor after PCI, works as well as 100 mg with similar safety for people staying on DAPT for 12 months.
-
Long-term P2Y12 inhibitor monotherapy and blood clotting after angioplasty
This trial will test whether specific P2Y12 drugs and reduced doses given alone keep platelet activity in a safe therapeutic range for people who completed initial dual antiplatelet therapy after PCI.
-
What affects bleeding control and how long you need to lie flat after femoral arterial sheath removal
We will see if patient and procedure factors can predict how long ICU patients need compression and bed rest after femoral arterial sheath removal to prevent bleeding and hematoma.
-
Doctors' and patients' preferences for PCI implantation devices
This questionnaire tests what patients who have had PCI and the doctors who treat them prefer between drug-eluting stents and drug-coated balloons.
-
How patients and doctors value different outcomes after coronary stent procedures
This project asks patients who had a coronary stent (PCI) and the doctors who treat them to rate how important different possible outcomes are to see if their priorities match.
-
Flozins to prevent contrast-related kidney injury after coronary angiography or PCI
This project tests whether taking a flozin (empagliflozin or dapagliflozin), short-term or long-term, lowers the chance of contrast-induced acute kidney injury in patients having coronary angiography or PCI.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.