Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
In patients with chronic coronary syndrome (CCS), clopidogrel has a class I/A indication in patients undergoing elective percutaneous coronary intervention (PCI). Although unproven, the possibility exists that clopidogrel does not yield an optimal platelet inhibition in multiple real-world scenarios that challenge current recommendations.
The aim of this prospective observational study io assess in a consecutive unselected series of patients with CCS undergoing elective PCI the frequency of the following real world clinical scenarios:
We expect to demonstrate:
In patients with chronic coronary syndrome (CCS), clopidogrel has a class I/A indication in patients undergoing elective percutaneous coronary intervention (PCI) (Figure 1). Initiation of oral P2Y12 inhibitors is usually delayed until the coronary anatomy is defined (Knuuti, Levine). Clopidogrel (administered as a 600 mg loading dose followed by a 75 mg maintenance dose) is the P2Y12 inhibitor of choice in CCS patients undergoing PCI (Knuuti, Levine). Also, pre-treatment with clopidogrel is currently recommended if the probability of PCI is high (II B/C). Although unproven, the possibility exists that clopidogrel does not yield an optimal platelet inhibition in multiple real-world scenarios that challenge current recommendations, as follows:
To assess in a consecutive unselected series of patients with CCS undergoing elective PCI the frequency of the following real world clinical scenarios:
Patients will be grouped as follows:
Pre-treatment with clopidogrel before elective PCI
Patients receiving a clopidogrel loading at time of elective PCI in the cath lab Patients receiving cangrelor during PCI in the cath lab and then receiving a P2Y12 inhibitor afterwards
Patients with CCS undergoing elective PCI
Patients' written informed and privacy consent obtained before the PCI procedure
Male or female patients 18 to 80 years old
Assessment of response to anti-platelet agents by VerifyNowTM
Patients with active bleeding
Patients with hypersensitivity to any anti-platelet agents or to any of its excipients
Known pregnancy or breast-feeding female patients > 1,000 patients Multicenter evaluation
Pre-treatment with clopidogrel before elective PCI
Patients receiving a clopidogrel loading at time of elective PCI in the cath lab
Patients receiving cangrelor during PCI in the cath lab and then receiving a P2Y12 inhibitor afterwards
1-year
Frequency of incomplete response to clopidogrel prior to elective PCI (as assessed by VerifyNow TM)
Frequency of the use of periprocedural i.v. cangrelor
Frequency of the use of glycoprotein IIb/IIIa (GPIIb/IIIa) inhibitors
Frequency of the use of clopidogrel, ticagrelor or prasugrel loading dose
Mode of administration of oral P2Y12 inhibitors (crushed)
Incidence of post-PCI ischemic complications
Incidence of any post-PCI bleeding according to the Bleeding Academic Research Consortium [BARC] criteria
Incidence of major adverse cardiac events (MACE) - MACE will comprise any of the following events: death, myocardial infarction (MI), ischemia-driven revascularisation (IDR) and stent thrombosis (ST)
Enrolment phase (1 year)
Follow-up: 1-year
The study will be conducted in accordance with the Declaration of Helsinki on ethical principles for medical research involving human subjects.
Informed consent to be included in this survey is mandatory for collecting individual data and must be obtained from all subjects and/or their legal representative(s) as per local regulations.
We expect to demonstrate:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Antiplatelet Agents | Drug | Antiplatelet agents more commonly used at time of percutaneous coronary intervention in patients with chronic coronary syndrome |
| Measure | Description | Time Frame |
|---|---|---|
| Frequency of 'naive' patients with CCS undergoing elective PCI | Number of 'naive' patients with CCS undergoing elective PCI | up to 12 months |
| Frequency of complex coronary intervention in patients undergoing elective PCI | Number of complex coronary intervention in patients undergoing elective PCI | up to 12 months |
Not provided
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Consecutive patients with CCS undergoing elective PCI.
Patients will be grouped as follows:
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Francesco Pelliccia, MD | Contact | +394997 | 123 | f.pelliccia@mclink.it |
| Carlo Gaudio, MD | Contact | +394997 | 123 |
| Name | Affiliation | Role |
|---|---|---|
| Francesco Pelliccia, MD | University Sapienza | Principal Investigator |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D003324 | Coronary Artery Disease |
| ID | Term |
|---|---|
| D003327 | Coronary Disease |
| D017202 | Myocardial Ischemia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D010975 | Platelet Aggregation Inhibitors |
| ID | Term |
|---|---|
| D006401 | Hematologic Agents |
| D045506 | Therapeutic Uses |
| D020228 | Pharmacologic Actions |
| D020164 | Chemical Actions and Uses |
Not provided
Not provided
Not provided
Not provided
Not provided
| D001161 |
| Arteriosclerosis |
| D001157 | Arterial Occlusive Diseases |
| D014652 | Vascular Diseases |