clopidogrel | Drug-Eluting Stent Implantation
Item
patients on clopidogrel therapy at 6 months (-1/+2 months) after des implantation
boolean
C0070166 (UMLS CUI [1])
C1322815 (UMLS CUI [2,1])
C0021107 (UMLS CUI [2,2])
Informed Consent
Item
informed, written consent by the patient
boolean
C0021430 (UMLS CUI [1])
Age
Item
age ≤18 years
boolean
C0001779 (UMLS CUI [1])
Symptoms Clinical Ischemia | Coronary Lesion by Angiographic Finding Requirement Revascularization
Item
clinically symptoms, proof of ischemia and/or presence of angiographic lesions requiring revascularization
boolean
C1457887 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C0022116 (UMLS CUI [1,3])
C3899494 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0581603 (UMLS CUI [2,3])
Stent thrombosis
Item
previous stent thrombosis
boolean
C3897493 (UMLS CUI [1])
Drug-Eluting Stent Left coronary artery
Item
des in left main coronary artery
boolean
C1322815 (UMLS CUI [1,1])
C1261082 (UMLS CUI [1,2])
ST segment elevation myocardial infarction | Non-ST elevation (NSTEMI) myocardial infarction
Item
st-elevation and non-st-elevation myocardial infarction during the last 6 months
boolean
C1536220 (UMLS CUI [1])
C1561921 (UMLS CUI [2])
Malignant Neoplasms | Comorbidity | Life Expectancy | Malignant Neoplasms Protocol Compliance Lacking | Comorbidity Protocol Compliance Lacking
Item
malignancies or other comorbid conditions with a life expectancy of less than one year or that may result in protocol noncompliance
boolean
C0006826 (UMLS CUI [1])
C0009488 (UMLS CUI [2])
C0023671 (UMLS CUI [3])
C0006826 (UMLS CUI [4,1])
C0525058 (UMLS CUI [4,2])
C0332268 (UMLS CUI [4,3])
C0009488 (UMLS CUI [5,1])
C0525058 (UMLS CUI [5,2])
C0332268 (UMLS CUI [5,3])
Major surgery Planned | Antiplatelet therapy To be stopped
Item
planned major surgery within the next 6 months with the need to discontinue antiplatelet therapy
boolean
C0679637 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C1096021 (UMLS CUI [2,1])
C1272691 (UMLS CUI [2,2])
Hemorrhage | Bleeding tendency | Intracranial Hemorrhages
Item
active bleeding; bleeding diathesis; history intracranial bleeding
boolean
C0019080 (UMLS CUI [1])
C1458140 (UMLS CUI [2])
C0151699 (UMLS CUI [3])
Anticoagulation Therapy Oral | Coumadin derivatives
Item
oral anticoagulation therapy with coumadin derivatives
boolean
C0003281 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0699129 (UMLS CUI [2,1])
C0243072 (UMLS CUI [2,2])
Hypersensitivity Investigational New Drugs | Intolerance to Investigational New Drugs | Aspirin allergy | Intolerance to Aspirin | Hypersensitivity clopidogrel | Intolerance to clopidogrel
Item
known allergy or intolerance to the study medications: aspirin and clopidogrel
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
C0004058 (UMLS CUI [3])
C1744706 (UMLS CUI [4,1])
C0004057 (UMLS CUI [4,2])
C0020517 (UMLS CUI [5,1])
C0070166 (UMLS CUI [5,2])
C1744706 (UMLS CUI [6,1])
C0070166 (UMLS CUI [6,2])
Pregnancy | Pregnancy Suspected | Pregnancy, Planned | Pregnancy test positive | Childbearing Potential Requirement Pregnancy test negative
Item
pregnancy (present, suspected or planned) or positive pregnancy test (in women with childbearing potential a negative 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])
C0427780 (UMLS CUI [5,3])
Protocol Compliance Unable
Item
patient's inability to fully comply with the study protocol
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Study Subject Participation Status
Item
prior enrollment in the same clinical trial.
boolean
C2348568 (UMLS CUI [1])