Multicentric Study on Clopidogrel Resistance in DAPT for CAS (MULTI-RESCLOSA)
MULTIcentric Study About RESistance to CLOpidogrel in Dual Antiplatelet Therapy for Carotid Stenting
IRCCS Policlinico S. Donato
1,140 participants
Sep 2, 2021
OBSERVATIONAL
Conditions
Summary
Spontaneous prospective observational multicentre pharmacological study that aims to evaluate whether, from a statistical point of view, there is a significant difference between the use of Ticagrelor in "non-responders" patients to Clopidogrel undergoing carotid stenting and Clopidogrel in "responders" undergoing carotid stenting, in the onset of death and major adverse cardiovascular events (MACE) and bleeding events, 1 and 3 months after the procedure. Furthermore, the study aims to evaluate the possible preoperative clinical and pharmacological factors most associated with the phenomenon of resistance to Clopidogrel. Inclusion criteria: The data will be collected on adult patients (age\> 18 years) who have given their consent to participate in the study, belonging to the U.O. of Vascular Surgery of the IRCCS Policlinico San Donato and the U.O. of Vascular Surgery of the participating centers and there subjected to the treatment of carotid stenosis by stenting technique. Exclusion criteria: Those patients who are minors, who have not given their consent to participate in the study, or who have carotid stenosis not susceptible to intervention by stenting will be excluded from the study. Pregnant or lactating women will also be excluded from the study (such as situations in which carotid stenting is contraindicated regardless of the execution of the study).
Eligibility
Inclusion Criteria2
- adult patients (age\> 18 years)
- patients who have given their consent to participate in the study, belonging to the U.O. of Vascular Surgery of the IRCCS Policlinico San Donato and the U.O. of Vascular Surgery of the participating centers and subjected to the treatment of carotid stenosis by stenting technique.
Exclusion Criteria4
- underage patients
- patients who have not given their consent to participate in the study,
- patients who have carotid stenosis not susceptible to intervention by stenting
- pregnant or lactating women (such as situations in which carotid stenting is contraindicated regardless of the execution of the study).
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Interventions
All patients will undergo carotid stenting and dual antiplatelet therapy with ASA + clopidogrel
All patients will undergo carotid stenting and dual antiplatelet therapy with ASA + clopidogrel
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05566301