Percutaneous Coronary Intervention Registry FRIBOURG
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age17-120
SponsorUniversity of Freiburg
About this trial
The registry aims to follow clinically all consecutive patients treated by percutaneous coronary interventions at hospital \& university Fribourg.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
All consecutive patients treated by percutaneous coronary intervention at our institution
Able to give informed consent and willing to participate
Disqualifiers
Unwillingness to participate
Enable to provide inform consent
Trial population
All comers
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Percutaneous coronary intervention, stents
Device
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
Patient-oriented composite endpoints (POCE)
Academic Research Consortium definition
Time frame
2 years2
Major Bleeding
Bleeding Academic Research Consortium definition
Time frame
2 years3
Patient-oriented composite endpoints (POCE)
Academic Research Consortium definition
Time frame
5 years4
Major Bleeding
Bleeding Academic Research Consortium definition
Time frame
5 yearsSecondary outcomes
1
all-cause death
Academic Research Consortium definition
Time frame
2 years2
any revascularization
Academic Research Consortium definition
Time frame
2 years3
any myocardial infarction
Academic Research Consortium definition
Time frame
2 yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov