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Recruiting NCT04185285

Percutaneous Coronary Intervention Registry FRIBOURG

Observational Coronary Artery Disease Percutaneous Coronary Intervention

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Percutaneous coronary intervention, stents.
Who it may be relevant to
Registry conditions: Coronary Artery Disease, Percutaneous Coronary Intervention. Basic parameters: 17 years — 120 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Switzerland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The registry aims to follow clinically all consecutive patients treated by percutaneous coronary interventions at hospital \& university Fribourg.

Interventions

  • Device Percutaneous coronary intervention, stents

Primary outcome measures

  • Patient-oriented composite endpoints (POCE) [Time frame: 2 years]
  • Major Bleeding [Time frame: 2 years]
  • Patient-oriented composite endpoints (POCE) [Time frame: 5 years]
  • Major Bleeding [Time frame: 5 years]
  • Patient-oriented composite endpoints (POCE) [Time frame: 10 years]
  • Major Bleeding [Time frame: 10 years]
Secondary outcome measures (3)
  • all-cause death [Time frame: 2 years]
  • any revascularization [Time frame: 2 years]
  • any myocardial infarction [Time frame: 2 years]

Eligibility 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Switzerland · 1 center
  • Cardiology, university Fribourg Medical Center — Fribourg

Publications

  • Cook ST, Allemann L, Cook M, Arroyo DA, Pittet T, Meier P, Togni M, Brahim-Mathiron A, Puricel S, Cook S. Sex differences in ST-segment elevation myocardial infarction patients treated by primary percutaneous intervention. Open Heart. 2025 Jan 4;12(1):e002831. doi: 10.1136/openhrt-2024-002831. PMID 39756819

Identifiers

NCT: NCT04185285 · 003-REP-CER-FR-2

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗