Informationen:
Fehler:
ID
28733
Beschreibung
Investigation of the Athero-Protective Effects of Clopidogrel; ODM derived from: https://clinicaltrials.gov/show/NCT01283282
Link
https://clinicaltrials.gov/show/NCT01283282
Stichworte
Versionen (1)
- 29.01.18 29.01.18 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
29. Januar 2018
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT01283282
Eligibility Coronary Artery Disease NCT01283282
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Coronary Artery Disease NCT01283282
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Gender | Childbearing Potential Absent | Age
Item
male or females without child bearing potential aged 21-80 years
boolean
C0079399 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0001779 (UMLS CUI [3])
C3831118 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0001779 (UMLS CUI [3])
Coronary Artery Disease Angiogram | Myocardial Infarction
Item
known coronary artery disease by angiogram or documented myocardial infarction.
boolean
C1956346 (UMLS CUI [1,1])
C0002978 (UMLS CUI [1,2])
C0027051 (UMLS CUI [2])
C0002978 (UMLS CUI [1,2])
C0027051 (UMLS CUI [2])
Informed Consent
Item
able to provide written informed consent
boolean
C0021430 (UMLS CUI [1])
Clopidogrel | Ticlopidine
Item
treated with clopidogrel or ticlodipine in the previous 3 months
boolean
C0070166 (UMLS CUI [1])
C0040207 (UMLS CUI [2])
C0040207 (UMLS CUI [2])
Age
Item
age < 21 or >80 years
boolean
C0001779 (UMLS CUI [1])
Premenopausal state Childbearing Potential
Item
premenopausal females with potential for pregnancy
boolean
C0232969 (UMLS CUI [1,1])
C3831118 (UMLS CUI [1,2])
C3831118 (UMLS CUI [1,2])
Hypersensitivity clopidogrel | Aspirin allergy
Item
allergy to clopidogrel or aspirin
boolean
C0020517 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
C0004058 (UMLS CUI [2])
C0070166 (UMLS CUI [1,2])
C0004058 (UMLS CUI [2])
Concomitant Therapy Initiation | Concomitant Therapy Medication dose changed
Item
initiation or change in dose of any concomitant medical therapy within 2 months before the study
boolean
C1707479 (UMLS CUI [1,1])
C1704686 (UMLS CUI [1,2])
C1707479 (UMLS CUI [2,1])
C1608430 (UMLS CUI [2,2])
C1704686 (UMLS CUI [1,2])
C1707479 (UMLS CUI [2,1])
C1608430 (UMLS CUI [2,2])
Uncontrolled hypertension | Systolic Pressure | Diastolic blood pressure
Item
uncontrolled hypertension with bp>180 mmhg systolic and >120 mmhg diastolic
boolean
C1868885 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Coumadin
Item
treated with coumadin therapy
boolean
C0699129 (UMLS CUI [1])
Intolerance to Statins | Hypersensitivity Statins
Item
intolerance or allergy to statins
boolean
C1744706 (UMLS CUI [1,1])
C0360714 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0360714 (UMLS CUI [2,2])
C0360714 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0360714 (UMLS CUI [2,2])
Communicable Disease
Item
acute infection in previous 4 weeks
boolean
C0009450 (UMLS CUI [1])
Substance Use Disorders
Item
history of substance abuse
boolean
C0038586 (UMLS CUI [1])
Tonometry Arterial Peripheral | Test Uninterpretable
Item
uninterpretable pat test
boolean
C0040420 (UMLS CUI [1,1])
C0221464 (UMLS CUI [1,2])
C0205100 (UMLS CUI [1,3])
C0039593 (UMLS CUI [2,1])
C3897243 (UMLS CUI [2,2])
C0221464 (UMLS CUI [1,2])
C0205100 (UMLS CUI [1,3])
C0039593 (UMLS CUI [2,1])
C3897243 (UMLS CUI [2,2])
Neoplasm
Item
current neoplasm
boolean
C0027651 (UMLS CUI [1])
Kidney Failure, Chronic | Creatinine measurement, serum | Liver Failure | Elevated liver enzymes
Item
chronic renal failure [creatinine > 2.5 mg/dl] or liver failure (liver enzymes >2x normal)
boolean
C0022661 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0085605 (UMLS CUI [3])
C0235996 (UMLS CUI [4])
C0201976 (UMLS CUI [2])
C0085605 (UMLS CUI [3])
C0235996 (UMLS CUI [4])
Acute Coronary Syndrome | Heart failure | Cerebrovascular accident | Intervention Coronary
Item
acute coronary syndrome, heart failure, cva, coronary intervention within 3 months
boolean
C0948089 (UMLS CUI [1])
C0018801 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0184661 (UMLS CUI [4,1])
C1522318 (UMLS CUI [4,2])
C0018801 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0184661 (UMLS CUI [4,1])
C1522318 (UMLS CUI [4,2])
Aortic Stenosis | Hypertrophic Cardiomyopathy | Heart failure Symptomatic
Item
known aortic stenosis, hypertrophic cardiomyopathy, symptomatic heart failure.
boolean
C0003507 (UMLS CUI [1])
C0007194 (UMLS CUI [2])
C0018801 (UMLS CUI [3,1])
C0231220 (UMLS CUI [3,2])
C0007194 (UMLS CUI [2])
C0018801 (UMLS CUI [3,1])
C0231220 (UMLS CUI [3,2])
Informed Consent Unable
Item
inability to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
Follow-up Availability Unable
Item
inability to return to emory for follow-up
boolean
C3274571 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0470187 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])