ID

34222

Beschrijving

Myovista iECG for Detecting Ischemic Heart Disease: Comparison With Computed Tomography Coronary Angiography; ODM derived from: https://clinicaltrials.gov/show/NCT01562730

Link

https://clinicaltrials.gov/show/NCT01562730

Trefwoorden

  1. 15-01-19 15-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

15 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT01562730

Eligibility Coronary Artery Disease NCT01562730

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
chest pain,
Beschrijving

ID.1

Datatype

boolean

shortness of breath,
Beschrijving

ID.2

Datatype

boolean

syncope or equivocal stress testing including exercise ecg,
Beschrijving

ID.3

Datatype

boolean

myocardial perfusion imaging, or stress echocardiography unable to exclude significant coronary artery disease.
Beschrijving

ID.4

Datatype

boolean

all patients will provide written and oral consent to ctca.
Beschrijving

ID.5

Datatype

boolean

patient agrees to participate and signs the informed consent
Beschrijving

ID.6

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
usually renal insufficiency (serum creatinine >120 mol/l),
Beschrijving

ID.7

Datatype

boolean

contraindications to the administration of iodinated contrast,
Beschrijving

ID.8

Datatype

boolean

pregnancy, acute coronary syndromes,
Beschrijving

ID.9

Datatype

boolean

and ventricular and/or supraventricular arrhythmias.
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Coronary Artery Disease NCT01562730

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
chest pain,
boolean
ID.2
Item
shortness of breath,
boolean
ID.3
Item
syncope or equivocal stress testing including exercise ecg,
boolean
ID.4
Item
myocardial perfusion imaging, or stress echocardiography unable to exclude significant coronary artery disease.
boolean
ID.5
Item
all patients will provide written and oral consent to ctca.
boolean
ID.6
Item
patient agrees to participate and signs the informed consent
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
usually renal insufficiency (serum creatinine >120 mol/l),
boolean
ID.8
Item
contraindications to the administration of iodinated contrast,
boolean
ID.9
Item
pregnancy, acute coronary syndromes,
boolean
ID.10
Item
and ventricular and/or supraventricular arrhythmias.
boolean

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