Percutaneous Coronary Intervention Registry FRIBOURG

University of Freiburg3,000 enrolled

Overview

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

Study Type

OBSERVATIONAL

Enrollment

3,000

Conditions

Coronary Artery Disease Percutaneous Coronary Intervention

Interventions

Percutaneous coronary intervention, stentsDEVICE

Eligibility

Sex: ALLMin age: 17 YearsMax age: 120 Years

Medical Language ↔ Plain English

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

Locations (1)

Cardiology, university Fribourg Medical Center

Fribourg, Switzerland

RECRUITING

Outcomes

Primary Outcomes

Patient-oriented composite endpoints (POCE)

Academic Research Consortium definition

Time frame: 2 years

Major Bleeding

Bleeding Academic Research Consortium definition

Time frame: 2 years

Patient-oriented composite endpoints (POCE)

Academic Research Consortium definition

Time frame: 5 years

Major Bleeding

Bleeding Academic Research Consortium definition

Time frame: 5 years

Patient-oriented composite endpoints (POCE)

Academic Research Consortium definition

Time frame: 10 years

Major Bleeding

Bleeding Academic Research Consortium definition

Time frame: 10 years

Secondary Outcomes

all-cause death

Academic Research Consortium definition

Time frame: 2 years

any revascularization

Academic Research Consortium definition

Time frame: 2 years

any myocardial infarction

Academic Research Consortium definition

Time frame: 2 years

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.