Age | Coronary Artery Disease Symptomatic | Percutaneous Coronary Intervention | Placement of stent
Item
patients older than 18 years with symptomatic coronary artery disease undergoing pci with stent implantation.
boolean
C0001779 (UMLS CUI [1])
C1956346 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C1532338 (UMLS CUI [3])
C0522776 (UMLS CUI [4])
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])
Shock, Cardiogenic
Item
cardiogenic shock.
boolean
C0036980 (UMLS CUI [1])
Malignant Neoplasms Protocol Compliance Lacking | Comorbidity Protocol Compliance Lacking | 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])
C0332268 (UMLS CUI [1,3])
C0009488 (UMLS CUI [2,1])
C0525058 (UMLS CUI [2,2])
C0332268 (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 Everolimus | Hypersensitivity Zotarolimus | Hypersensitivity Cobalt Chrome
Item
known allergy to the study medications: everolimus, zotarolimus, cobalt chrome.
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0541315 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C1700035 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0008576 (UMLS CUI [4,2])
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 | Childbearing Potential Requirement Pregnancy Test
Item
pregnancy (present, suspected or planned) or positive pregnancy test. (in women with childbearing potential a pregnancy test is mandatory.)
boolean
C0032961 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0032992 (UMLS CUI [3])
C0240802 (UMLS CUI [4])
C3831118 (UMLS CUI [5,1])
C1514873 (UMLS CUI [5,2])
C0032976 (UMLS CUI [5,3])
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])