Age | Symptoms Ischemic | Myocardial Ischemia | De novo stenosis Percentage | Location Coronary Vessels Native
Item
patients older than age 18 with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥ 50% de novo stenosis located in native coronary vessels
boolean
C0001779 (UMLS CUI [1])
C1457887 (UMLS CUI [2,1])
C0475224 (UMLS CUI [2,2])
C0151744 (UMLS CUI [3])
C4264488 (UMLS CUI [4,1])
C0439165 (UMLS CUI [4,2])
C1515974 (UMLS CUI [5,1])
C0010075 (UMLS CUI [5,2])
C0302891 (UMLS CUI [5,3])
Informed Consent | Informed Consent Patient Representative
Item
written, informed consent by the patient or her/his legally-authorized representative for participation in the study
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
Childbearing Potential Pregnancy test negative
Item
in women with childbearing potential a negative pregnancy test is mandatory.
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
Target Lesion Location Trunk of left coronary artery Main
Item
target lesion located in the left main trunk.
boolean
C2986546 (UMLS CUI [1,1])
C1515974 (UMLS CUI [1,2])
C0920980 (UMLS CUI [1,3])
C1542147 (UMLS CUI [1,4])
Target Lesion Location Bypass graft
Item
target lesion located in the bypass graft.
boolean
C2986546 (UMLS CUI [1,1])
C1515974 (UMLS CUI [1,2])
C0185098 (UMLS CUI [1,3])
In Stent restenosis
Item
in-stent restenosis.
boolean
C3272317 (UMLS CUI [1])
Shock, Cardiogenic
Item
cardiogenic shock.
boolean
C0036980 (UMLS CUI [1])
Malignant Neoplasms Protocol Compliance Unable | Comorbidity Protocol Compliance Unable | Life Expectancy | Liver disease Severe | Kidney Disease Severe | Pancreatic Disease Severe
Item
malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than 12 months or that may result in protocol non-compliance.
boolean
C0006826 (UMLS CUI [1,1])
C0525058 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0009488 (UMLS CUI [2,1])
C0525058 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
C0023671 (UMLS CUI [3])
C0023895 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0022658 (UMLS CUI [5,1])
C0205082 (UMLS CUI [5,2])
C0030286 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])
Hypersensitivity Investigational New Drugs | Hypersensitivity clopidogrel | Hypersensitivity Rapamycin | Probucol allergy | Hypersensitivity zotarolimus | Hypersensitivity Stainless Steel | Hypersensitivity Cobalt Chrome
Item
known allergy to the study medications: clopidogrel, rapamycin, probucol, zotarolimus, stainless steel or cobalt chrome.
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0072980 (UMLS CUI [3,2])
C0571861 (UMLS CUI [4])
C0020517 (UMLS CUI [5,1])
C1700035 (UMLS CUI [5,2])
C0020517 (UMLS CUI [6,1])
C0038126 (UMLS CUI [6,2])
C0020517 (UMLS CUI [7,1])
C0008576 (UMLS CUI [7,2])
Clopidogrel Intake Unable
Item
inability to take clopidogrel for at least 6 months.
boolean
C0070166 (UMLS CUI [1,1])
C1512806 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Pregnancy | Pregnancy Suspected | Pregnancy, Planned | Pregnancy test positive
Item
pregnancy (present, suspected or planned) or positive pregnancy test.
boolean
C0032961 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0032992 (UMLS CUI [3])
C0240802 (UMLS CUI [4])
Study Subject Participation Status
Item
previous enrollment in this trial.
boolean
C2348568 (UMLS CUI [1])
Protocol Compliance Unable
Item
patient's inability to fully cooperate with the study protocol.
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])