Informed Consent
Item
able and willing to provide informed consent
boolean
C0021430 (UMLS CUI [1])
Gender | Age | Racial group Any
Item
women at least 45 years old of any race
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0034510 (UMLS CUI [3,1])
C1552551 (UMLS CUI [3,2])
Aspirin U/day
Item
taking 81 mg aspirin daily, for at least one month
boolean
C0004057 (UMLS CUI [1,1])
C0456683 (UMLS CUI [1,2])
Coronary Artery Disease | Coronary Artery Disease Suspected | Lesion Quantity Stenosis Percentage | Angiography | Troponin increased | Creatine kinase MB increased | ECG changes Leads Quantity | ST depression New | ST elevation Transient | Coronary revascularisation PCI | Coronary revascularisation CABG
Item
diagnosed with known or suspected cad with at least one of the following: angiographic evidence of at least one lesion > 50% stenosis, history of significant elevation of biomarker troponin or ck-mb, or history of ecg changes in at least 2 contiguous leads characterized by either new st depression > 0.1 mv or transient (<30 min) st elevation > 0.1 mv, coronary artery revascularization either by pci or cabg
boolean
C1956346 (UMLS CUI [1])
C1956346 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0221198 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C1261287 (UMLS CUI [3,3])
C0439165 (UMLS CUI [3,4])
C0002978 (UMLS CUI [4])
C1141948 (UMLS CUI [5])
C0861005 (UMLS CUI [6])
C0855329 (UMLS CUI [7,1])
C0181586 (UMLS CUI [7,2])
C1265611 (UMLS CUI [7,3])
C0520887 (UMLS CUI [8,1])
C0205314 (UMLS CUI [8,2])
C0520886 (UMLS CUI [9,1])
C0205374 (UMLS CUI [9,2])
C0877341 (UMLS CUI [10,1])
C1532338 (UMLS CUI [10,2])
C0877341 (UMLS CUI [11,1])
C0010055 (UMLS CUI [11,2])
Age
Item
< 45 years or > 85 years of age
boolean
C0001779 (UMLS CUI [1])
Unstable status Clinical | Hypotension | Systolic Pressure | Heart failure Associated with Symptoms | Pulmonary Edema Unstable | Pulmonary Edema Severe | CONGESTIVE HEART FAILURE DECOMPENSATED | Mitral Valve Insufficiency | Ventricular Septal Defects | Cerebrovascular accident | Transient Ischemic Attack | Ventricular Fibrillation | Implantable defibrillator Absent | Supraventricular tachycardia Duration | Supraventricular tachycardia Associated with Symptoms | Complete atrioventricular block Untreated | Heart Block Secondary Severe Untreated
Item
clinically unstable: hypotension defined as sustained systolic blood pressure of <90 mmhg due to cardiac failure with associated symptoms, unstable or severe pulmonary edema, decompensated congestive heart failure, acute mitral regurgitation, acute ventricular septal defect, acute cerebrovascular event or transient ischemic attack (tia) within the past six months, history of ventricular fibrillation and no implantable cardioverter defibrillator (icd), sustained supraventricular tachycardia > 30 seconds or associated with symptoms and no icd, untreated complete heart block or untreated high grade secondary heart block
boolean
C0443343 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C0020649 (UMLS CUI [2])
C0871470 (UMLS CUI [3])
C0018801 (UMLS CUI [4,1])
C0332281 (UMLS CUI [4,2])
C1457887 (UMLS CUI [4,3])
C0034063 (UMLS CUI [5,1])
C0443343 (UMLS CUI [5,2])
C0034063 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])
C0742746 (UMLS CUI [7])
C0026266 (UMLS CUI [8])
C0018818 (UMLS CUI [9])
C0038454 (UMLS CUI [10])
C0007787 (UMLS CUI [11])
C0042510 (UMLS CUI [12])
C0162589 (UMLS CUI [13,1])
C0332197 (UMLS CUI [13,2])
C0039240 (UMLS CUI [14,1])
C0449238 (UMLS CUI [14,2])
C0039240 (UMLS CUI [15,1])
C0332281 (UMLS CUI [15,2])
C1457887 (UMLS CUI [15,3])
C0151517 (UMLS CUI [16,1])
C0332155 (UMLS CUI [16,2])
C0018794 (UMLS CUI [17,1])
C0175668 (UMLS CUI [17,2])
C0205082 (UMLS CUI [17,3])
C0332155 (UMLS CUI [17,4])
Pregnancy | Pregnancy, Planned | Breast Feeding
Item
pregnant, planning to become pregnant, or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Alcohol abuse | DRUG ABUSE ILLICIT
Item
alcohol abuse or illicit drug abuse
boolean
C0085762 (UMLS CUI [1])
C0743253 (UMLS CUI [2])
Salicylate allergy | Intolerance to Salicylate | Hypersensitivity Salicylate Excipient | Intolerance to Salicylate Excipient | Gastrointestinal Hemorrhage
Item
allergy or intolerance to salicylates and/or excipients including a history of and/or active gi bleed
boolean
C0570514 (UMLS CUI [1])
C1744706 (UMLS CUI [2,1])
C0036075 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0036075 (UMLS CUI [3,2])
C0015237 (UMLS CUI [3,3])
C1744706 (UMLS CUI [4,1])
C0036075 (UMLS CUI [4,2])
C0015237 (UMLS CUI [4,3])
C0017181 (UMLS CUI [5])
NSAIDs | NSAIDs Regular Planned
Item
use of nsaids within seven days or planned regular use during the study
boolean
C0003211 (UMLS CUI [1])
C0003211 (UMLS CUI [2,1])
C0205272 (UMLS CUI [2,2])
C1301732 (UMLS CUI [2,3])
Hormone replacement therapy | Contraceptives, Oral | Hormone replacement therapy Planned | Oral Contraceptives Planned
Item
taking hrt or oral contraceptives within the past 30 days or planned use during study
boolean
C0282402 (UMLS CUI [1])
C0009905 (UMLS CUI [2])
C0282402 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
C0009905 (UMLS CUI [4,1])
C1301732 (UMLS CUI [4,2])
Heparin | Warfarin | Adenosine Diphosphate Receptor Inhibitors | clopidogrel | prasugrel | Ticlopidine | Platelet Glycoprotein IIb/IIIA Inhibitors
Item
use of heparin, warfarin, adp inhibitors (clopidogrel, prasugrel, or ticlopidine), or glycoprotein iib/iia inhibitors within previous 96 hours or planned use during the study
boolean
C0019134 (UMLS CUI [1])
C0043031 (UMLS CUI [2])
C1373149 (UMLS CUI [3])
C0070166 (UMLS CUI [4])
C1620287 (UMLS CUI [5])
C0040207 (UMLS CUI [6])
C1373125 (UMLS CUI [7])
Pharmaceutical Preparations Interfere with Arachidonic acid induced platelet aggregation
Item
use or planned use of any other medications known to interfere with aa-induced platelet function
boolean
C0013227 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C1268820 (UMLS CUI [1,3])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
currently participating in another investigational drug or device study
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Life Expectancy
Item
survival less than six months
boolean
C0023671 (UMLS CUI [1])