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NCT04185285 Clinical Trial

Percutaneous Coronary Intervention Registry FRIBOURG

Coronary Artery Disease Clinical Trial

— Cardio-FR  

Official title:
Percutaneous Coronary Intervention Registry FRIBOURG

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04185285
Other study ID # 003-REP-CER-FR-2
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 1, 2015
Est. completion date September 1, 2027

Study information
Verified date October 2021
Source University of Freiburg
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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

Recruitment information / eligibility
Status Recruiting
Enrollment 3000
Est. completion date September 1, 2027
Est. primary completion date September 1, 2017
Accepts healthy volunteers No
Gender All
Age group 17 Years to 120 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Percutaneous coronary intervention, stents

Locations
Country Name City State
Switzerland Cardiology, university Fribourg Medical Center Fribourg

Sponsors (1)
Lead Sponsor Collaborator
University of Freiburg

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Patient-oriented composite endpoints (POCE) Academic Research Consortium definition 2 years
Primary Major Bleeding Bleeding Academic Research Consortium definition 2 years
Primary Patient-oriented composite endpoints (POCE) Academic Research Consortium definition 5 years
Primary Major Bleeding Bleeding Academic Research Consortium definition 5 years
Primary Patient-oriented composite endpoints (POCE) Academic Research Consortium definition 10 years
Primary Major Bleeding Bleeding Academic Research Consortium definition 10 years
Secondary all-cause death Academic Research Consortium definition 2 years
Secondary any revascularization Academic Research Consortium definition 2 years
Secondary any myocardial infarction Academic Research Consortium definition 2 years
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