Age, ischemic symptoms or evidence of myocardial ischemia, coronary vessel stenosis
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])
C0151744 (UMLS CUI [2])
C0242231 (UMLS CUI [3])
informed consent
Item
written, informed consent by the patient or her/his legally-authorized representative for participation in the study.
boolean
C0021430 (UMLS CUI [1])
target lesion located in the left main trunk or bypass graft
Item
target lesion located in the left main trunk or bypass graft.
boolean
C2184261 (UMLS CUI [1,1])
C0226069 (UMLS CUI [1,2])
C2184261 (UMLS CUI [2,1])
C0185098 (UMLS CUI [2,2])
In-stent restenosis
Item
in-stent restenosis.
boolean
C3272317 (UMLS CUI [1])
acute st-elevation myocardial infarction
Item
acute st-elevation myocardial infarction.
boolean
C1303258 (UMLS CUI [1])
Cardiogenic shock
Item
cardiogenic shock.
boolean
C0036980 (UMLS CUI [1])
Comorbidity
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
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Allergy to the study medications
Item
known allergy to the study medications: aspirin, clopidogrel, rapamycin, estradiol, stainless steel.
boolean
C0020517 (UMLS CUI [1,1])
C3854006 (UMLS CUI [1,2])
Pregnancy
Item
pregnancy (present, suspected or planned) or positive pregnancy test.
boolean
C0032961 (UMLS CUI [1])
Previous enrollment in this trial
Item
previous enrollment in this trial.
boolean
C2348568 (UMLS CUI [1])
inability to cooperate with the study protocol
Item
patient's inability to fully cooperate with the study protocol.
boolean
C2348563 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])