Clinical trial Recruiting at 1 site Observational Ages 17 to 120

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.

More Coronary Artery Disease trials

Quick facts

Study typeObservational
Ages17 Years to 120 Years
SexAll
Enrollment3000 (estimated)
SponsorUniversity of Freiburg
Academic / other
Locations1 site (Fribourg)
StatusRecruiting
StartedMay 1, 2015
Main results expectedSeptember 1, 2017
Study endsSeptember 1, 2027
Registry record updatedOctober 22, 2021
Trial IDNCT04185285 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

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.