Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:17 AM
Ignite Modification Date:
2025-12-25 @ 3:17 AM
NCT ID:
NCT03184805
Eligibility Criteria:
Inclusion Criteria:
* Age 19-85 years
* Planning of elective noncardiac surgery or invasive procedure
* At least 1 year interval between the surgery or procedure and last PCI with next generation DES
* Currently on antiplatelet therapy
Exclusion Criteria:
* PCI with BMS(bare metal stent), 1st generation DES or bioresorbable vascular scaffold
* Total length of inserted DES in the 3 vessels \>60 mm
* History of stent thrombosis
* History of coronary artery bypass grafting surgery
* Planned surgery or procedure with high bleeding risk including followings: intracranial neurosurgery, spinal canal surgery, and eye posterior chamber surgery, endoscopic mucosal resection (EMR), endoscopic submucosal dissection (ESD), ampullary resection, endoscopic retrograde cholangiopancreatography (ERCP) with endoscopic sphincterotomy plus large-balloon papillary dilation, endoscopic ultrasonography-guided fine-needle aspiration (EUS-FNA) of cystic lesions
* Left ventricular ejection fraction \<40%
* Myocardial infarction within 6 months
* Any overt thromboembolism requiring medical surveillance and/or treatment
* Any clinically overt sign of hemorrhage within 3 months
* Anticoagulant therapy for any reason
* Need of continuation or discontinuation of antiplatelet therapy during surgery or procedure at the discretion of cardiologist or operator
* Any contraindication, adverse drug reaction or hypersensitivity to aspirin
* Pregnant women or women with potential childbearing
* Inability to understand or read the informed content
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
19 Years
Maximum Age:
85 Years
Study:
NCT03184805
Study Brief:
Protocol Section:
NCT03184805