Bifurcation lesion of coronary artery de novo Classification | Exception Classification
Item
de novo bifurcation lesions following the medina classification except (0,0,1).
boolean
C1299363 (UMLS CUI [1,1])
C1515568 (UMLS CUI [1,2])
C0008902 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C0008902 (UMLS CUI [2,2])
Bifurcation lesion of coronary artery Quantity Maximum
Item
maximum one bifurcation lesion per patient.
boolean
C1299363 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
Bifurcation Lesion Single per Vessel
Item
single bifurcation lesion per vessel.
boolean
C3640041 (UMLS CUI [1,1])
C0205171 (UMLS CUI [1,2])
C3887962 (UMLS CUI [1,3])
C0005847 (UMLS CUI [1,4])
Age | Myocardial Ischemia | Stable angina | Angina, Unstable | Silent myocardial ischemia | Test Functional Positive
Item
the patient is at least 18 years of age. the patient has clinical evidence of ischemic heart disease, stable or unstable angina, silent ischemia, or a positive functional trial.
boolean
C0001779 (UMLS CUI [1])
C0151744 (UMLS CUI [2])
C0340288 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
C0340291 (UMLS CUI [5])
C0039593 (UMLS CUI [6,1])
C0205245 (UMLS CUI [6,2])
C1514241 (UMLS CUI [6,3])
Patient Appropriate PTCA | Patient Appropriate Stenting | Patient Appropriate Emergency Coronary Artery Bypass Surgery
Item
the patient is an acceptable candidate for percutaneous transluminal coronary angioplasty (ptca), stenting, and emergent coronary artery bypass graft (cabg) surgery.
boolean
C0030705 (UMLS CUI [1,1])
C1548787 (UMLS CUI [1,2])
C2936173 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C1548787 (UMLS CUI [2,2])
C2348535 (UMLS CUI [2,3])
C0030705 (UMLS CUI [3,1])
C1548787 (UMLS CUI [3,2])
C0013956 (UMLS CUI [3,3])
C0010055 (UMLS CUI [3,4])
Protocol Compliance | Protocol Compliance Patient Representative | Informed Consent | Informed Consent Patient Representative
Item
the patient or patient's legal representative has been informed of the nature of the trial and agrees to its provisions and has provided written informed consent as approved by the institutional review board/ethics committee (irb/ec) of the respective clinical site.
boolean
C0525058 (UMLS CUI [1])
C0525058 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3])
C0021430 (UMLS CUI [4,1])
C0030701 (UMLS CUI [4,2])
Agreement Follow-up visit
Item
the patient agrees to return to the same research facility for all required post-procedure follow-up visits.
boolean
C0680240 (UMLS CUI [1,1])
C0589121 (UMLS CUI [1,2])
Bifurcation lesion of coronary artery de novo Classification
Item
de novo bifurcation lesion medina (0,0,1).
boolean
C1299363 (UMLS CUI [1,1])
C1515568 (UMLS CUI [1,2])
C0008902 (UMLS CUI [1,3])
Left Main Coronary Artery Bifurcation
Item
left main bifurcation.
boolean
C3898614 (UMLS CUI [1])
Lesion Calcified Severe
Item
heavily calcified lesions.
boolean
C0221198 (UMLS CUI [1,1])
C0175895 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
Lesion Tortuous Severe
Item
severe tortuous lesions.
boolean
C0221198 (UMLS CUI [1,1])
C4068863 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
Left ventricular ejection fraction
Item
documented left ventricular ejection fraction (lvef) < 30% at most recent evaluation.
boolean
C0428772 (UMLS CUI [1])
Childbearing Potential
Item
women of childbearing potential.
boolean
C3831118 (UMLS CUI [1])
Chronic Total Occlusion
Item
chronic total occlusion (cto).
boolean
C3275069 (UMLS CUI [1])
Percutaneous Coronary Intervention Target Lesion
Item
previous pci of the target lesion.
boolean
C1532338 (UMLS CUI [1,1])
C2986546 (UMLS CUI [1,2])
Lesion second Target vessel | Treatment required for
Item
second lesion requiring treatment in target vessel.
boolean
C0221198 (UMLS CUI [1,1])
C0205436 (UMLS CUI [1,2])
C0449618 (UMLS CUI [1,3])
C0332121 (UMLS CUI [2])
Bifurcation lesion of coronary artery second Treatment required for
Item
second bifurcation lesion requiring treatment.
boolean
C1299363 (UMLS CUI [1,1])
C0205436 (UMLS CUI [1,2])
C0332121 (UMLS CUI [1,3])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device | Primary Endpoint Incomplete | Interference Endpoints Current | Patient need for Coronary angiography | Patient need for IVUS | Patient need for Coronary artery Imaging
Item
currently participating in an investigational drug or another device trial that has not completed the primary endpoint or that clinically interferes with the current trial endpoints; or requires coronary angiography, ivus or other coronary artery imaging procedures.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
C2986535 (UMLS CUI [4,1])
C0205257 (UMLS CUI [4,2])
C0521102 (UMLS CUI [5,1])
C2349179 (UMLS CUI [5,2])
C0521116 (UMLS CUI [5,3])
C0686904 (UMLS CUI [6,1])
C0085532 (UMLS CUI [6,2])
C0686904 (UMLS CUI [7,1])
C0206520 (UMLS CUI [7,2])
C0686904 (UMLS CUI [8,1])
C0205042 (UMLS CUI [8,2])
C0011923 (UMLS CUI [8,3])