Informed Consent
Item
provision of informed consent prior to any study specific procedures;
boolean
C0021430 (UMLS CUI [1])
Age
Item
men and women 18 years and older;.
boolean
C0001779 (UMLS CUI [1])
Indication Percutaneous Coronary Intervention | American Heart Association Guidelines
Item
established indication to pci according to the guidelines of american heart association and american college of cardiology;
boolean
C3146298 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
C0002458 (UMLS CUI [2,1])
C0162791 (UMLS CUI [2,2])
Coronary Vessel Lesion Native | Amenable Drug-eluting coronary stent placement
Item
native coronary lesion suitable for drug-eluting stent placement;
boolean
C3272304 (UMLS CUI [1,1])
C0302891 (UMLS CUI [1,2])
C3900053 (UMLS CUI [2,1])
C2609296 (UMLS CUI [2,2])
Bifurcation lesion of coronary artery
Item
true bifurcation lesions (medina 0,1,1/1,1,1 /1,0,1);
boolean
C1299363 (UMLS CUI [1])
Mean Vessel Diameter | Visual estimation
Item
reference vessel diameter in side branch ≥2.5mm by visual estimation.
boolean
C3898449 (UMLS CUI [1])
C0444684 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnancy and breast feeding mother;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Comorbidity | Life Expectancy
Item
co-morbidity with an estimated life expectancy of < 50 % at 12 months;
boolean
C0009488 (UMLS CUI [1])
C0023671 (UMLS CUI [2])
Major surgery Scheduled
Item
scheduled major surgery in the next 12 months;
boolean
C0679637 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
Compliance behavior Limited
Item
inability to follow the protocol and comply with follow-up requirements or any other reason that the investigator feels would place the patient at increased risk;
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
Study Subject Participation Status | Therapeutic procedure Investigational New Drugs | Therapeutic procedure Investigational Medical Device
Item
previous enrolment in this study or treatment with an investigational drug or device under another study protocol in the past 30 days;
boolean
C2348568 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
C0087111 (UMLS CUI [3,1])
C2346570 (UMLS CUI [3,2])
Hypersensitivity Ticagrelor | Hypersensitivity clopidogrel | History of chronic use of aspirin Hemorrhage Major | Intracranial Hemorrhages | Gastrointestinal Hemorrhage
Item
known allergy against ticagrelor, or against clopidogrel, or aspirin history of major hemorrhage (intracranial, gastrointestinal, etc.);
boolean
C0020517 (UMLS CUI [1,1])
C1999375 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C2054132 (UMLS CUI [3,1])
C0019080 (UMLS CUI [3,2])
C0205164 (UMLS CUI [3,3])
C0151699 (UMLS CUI [4])
C0017181 (UMLS CUI [5])
chronic total occlusion Anterior descending branch of left coronary artery | chronic total occlusion Structure of circumflex branch of left coronary artery | chronic total occlusion Entire right coronary artery | recanalized
Item
chronic total occlusion lesion in either lad, or lcx or rca not re-canalized;
boolean
C3275069 (UMLS CUI [1,1])
C0226032 (UMLS CUI [1,2])
C3275069 (UMLS CUI [2,1])
C0226037 (UMLS CUI [2,2])
C3275069 (UMLS CUI [3,1])
C0226042 (UMLS CUI [3,2])
C0333328 (UMLS CUI [4])
Calcification Severe Needs Rotational Atherectomy
Item
severe calcification needing rotational atherectomy;
boolean
C0175895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0027552 (UMLS CUI [1,3])
C0162655 (UMLS CUI [1,4])
ST segment elevation myocardial infarction | Chest Pain
Item
patient with stemi (within 24-hour from the onset of chest pain to admission).
boolean
C1536220 (UMLS CUI [1])
C0008031 (UMLS CUI [2])