Age | Symptoms Ischemic | Myocardial Ischemia Evidence of | Stenosis de novo Coronary Vessels
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 [3,1])
C0332120 (UMLS CUI [3,2])
C1261287 (UMLS CUI [4,1])
C1515568 (UMLS CUI [4,2])
C0010075 (UMLS CUI [4,3])
Informed Consent | Informed Consent Patient Representatives
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])
Target Lesion Identification Left coronary artery main stem | Bypass graft
Item
target lesion located in the left main trunk or bypass graft.
boolean
C2986546 (UMLS CUI [1,1])
C0226031 (UMLS CUI [1,2])
C0185098 (UMLS CUI [2])
In-stent coronary artery restenosis
Item
in-stent restenosis.
boolean
C1868718 (UMLS CUI [1])
Shock, Cardiogenic
Item
cardiogenic shock.
boolean
C0036980 (UMLS CUI [1])
Malignant Neoplasms | Comorbidity Protocol Compliance Unable | Liver disease Severe | Kidney Disease Severe | Pancreatic Disease Severe | Life Expectancy
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])
C0009488 (UMLS CUI [2,1])
C0525058 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
C0023895 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0022658 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0030286 (UMLS CUI [5,1])
C0205082 (UMLS CUI [5,2])
C0023671 (UMLS CUI [6])
Hypersensitivity Investigational New Drugs | Aspirin allergy | Hypersensitivity clopidogrel | Hypersensitivity Sirolimus | Hypersensitivity Stainless Steel
Item
known allergy to the study medications: aspirin, clopidogrel, rapamycin, stainless steel.
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0004058 (UMLS CUI [2])
C0020517 (UMLS CUI [3,1])
C0070166 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0072980 (UMLS CUI [4,2])
C0020517 (UMLS CUI [5,1])
C0038126 (UMLS CUI [5,2])
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])