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:
2025-12-24 @ 10:17 PM
Ignite Modification Date:
2025-12-24 @ 10:17 PM
NCT ID:
NCT02224235
Eligibility Criteria:
Inclusion Criteria:
* Patient \>= 18 years old.
* Eligible for percutaneous coronary intervention (PCI).
* Patient provides written informed consent.
* Patient is willing to comply with follow-up evaluation.
* Acceptable candidate for coronary artery bypass graft (CABG) surgery.
* Stable angina pectoris or a positive functional ischemia study.
* Male or non-pregnant female patient
* Patient indicated for elective stenting of up to 2 stenotic lesions in two separate native coronary arteries.
* Reference vessel \>=2.5 mm and\<= 4.0 mm in diameter by visual estimate.
* Target lesion \<=20 mm in length by visual estimate.
* Protected left main lesion with \>50% stenosis.
* Target lesion stenosis \>= 70% and \< 100% by visual estimate OR Target lesion stenosis \<70% who meet physiological criteria for revascularization (i.e. positive Fractional Flow Reserve).
Exclusion Criteria:
* Currently enrolled in another investigational device or drug trial.
* Previously enrolled in another stent trial within the prior 2 years.
* ANY planned elective surgery or percutaneous intervention within the subsequent 3 months.
* A previous coronary interventional procedure of any kind within 30 days prior to the procedure.
* The patient requires staged procedure of either the target or any non-target vessel before OCT procedure at 3 months post-procedure.
* The target lesion requires treatment with a device other than percutaneous transluminal coronary angioplasty (PTCA) prior to stent placement.
* Previous drug eluting stent (DES) or bare metal stent (BMS) deployment anywhere in the target vessel.
* Co-morbid condition(s) that could limit the patient's ability to participate in the trial or to comply with follow-up requirements, or impact the scientific integrity of the trial.
* Concurrent medical condition with a life expectancy of less than 12 months.
* Documented left ventricular ejection fraction (LVEF) \< 50% at the most recent evaluation.
* Patients with diagnosis of myocardial infarction (MI) within 72 hours (i.e. CK-MB must be returned to normal prior to enrollment) or suspected acute MI at time of enrollment.
* Previous intervention in the target vessel.
* History of cerebrovascular accident or transient ischemic attack in the last 6 months.
* Leukopenia (leukocytes \< 3.5 x10\^9 / liter).
* Neutropenia (Absolute Neutrophil Count \< 1000/mm3) \<= 3 days prior to enrollment.
* Thrombocytopenia (platelets \< 100,000/mm3) pre-procedure.
* Active peptic ulcer or active GI bleeding.
* History of bleeding diathesis or coagulopathy or inability to accept blood transfusions.
* Known hypersensitivity or contraindication to aspirin, heparin or bivalirudin, clopidogrel or ticlopidine, cobalt, nickel, L-605 Cobalt chromium alloy or sensitivity to contrast media, which cannot be adequately pre-medicated.
* Serum creatinine level \> 2.0 mg/dl within 7 days prior to index procedure.
* Patients not responsive to Plavix/ aspirin and or unable to tolerate Plavix/ aspirin for 6 month post procedure.
* Patient on or may require anticoagulation therapy within 3 months of index procedure.
* Flow limiting dissections observed on OCT
* Significant tissue prolapse within the stent observed on OCT
* Unprotected left main coronary artery disease
* Target vessel with any lesions with greater than 60% diameter stenosis outside of a range of 5 mm proximal and distal to the target lesion based on visual estimate or on-line quantitative coronary arteriography (QCA).
* Target lesion (or vessel) exhibiting an intraluminal thrombus (occupying \> 50% of the true lumen diameter) at any time.
* Lesion location that is aorto-ostial or within 5 mm of the origin of the left anterior descending (LAD) or left circumflex (LCX).
* Target lesion with side branches \> 2.0mm in diameter.
* Target vessel is excessively tortuous (two bends \> 90˚ to reach the target lesion).
* Target lesion is severely calcified.
* Thrombolysis In Myocardial Infarction (TIMI) flow 0 or 1
* Target lesion is in a bypass graft
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02224235
Study Brief:
Protocol Section:
NCT02224235