P2Y12 Inhibitors Utilization in Bifurcation and Chronic Total Occlusion PCI
- Conditions
- Coronary Arteriosclerosis
- Registration Number
- NCT01967615
- Lead Sponsor
- G. d'Annunzio University
- Brief Summary
Prasugrel and ticagrelor were both associated with a significant reduction in the risk of MACE in patients undergoing PCI for an ACS, mostly through a reduced stent thrombosis. The 1-year relative risk reduction (RRR) of definite of probable stent thrombosis in patients receiving a DES were fairly different in TRITON-TIMI 38 and PLATO trials. The incidence of "biologically active" stent (DES or BVS) thrombosis is largely variable according to different lesion settings. We aim to verify the translation of the postulated different reduction in thrombosis rate among various P2Y12 inhibitors (clopidogrel, prasugrel and ticagrelor) in a high-risk setting such as the PCI with DES or BVS in CTO and bifurcating lesions.
- Detailed Description
All patients aged 18-80 who underwent PCI of a CTO or bifurcating lesion (all Medina types, side branch ≥2 mm) with "biologically active stents" (DES or BVS) between January 2012 and december 2014 at participating centers will be deemed eligible to enter the registry.
In-hospital outcomes will be recorded; all patients discharged alive will be followed up with a telephone interview (minimum follow-up 6 months).
The primary end-point will be the occurrence of a cluster of major adverse cardiovascular events at 1 year:
1. Death from any cause.
2. Myocardial infarction.
3. Stent thrombosis, defined as definite, probable or possible following the Academic Research Consortium.
Sample size 3150 patients.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 4500
- Age between 18-80 years old
- PCI of a CTO or bifurcating lesion (all Medina types, side branch ≥2 mm) with "biologically active stents"
-none
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Death, Myocardial infarction, Stent Thrombosis 30 months 1. Death from any cause.
2. Myocardial infarction, defined as an elevation of the creatine kinase MB fraction or cardiac troponins by a factor of 3 or more, or the development of new Q waves in 2 or more contiguous leads at surface ECG7. Levels of total creatine kinase and the creatine kinase MB fraction will be measured in all patients between 12 and 24 hours after PCI.
3. Stent thrombosis, defined as definite, probable or possible3 following the Academic Research Consortium
- Secondary Outcome Measures
Name Time Method