ID

34222

Description

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

Keywords

  1. 1/15/19 1/15/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 15, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT01562730

Eligibility Coronary Artery Disease NCT01562730

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
chest pain,
Description

ID.1

Data type

boolean

shortness of breath,
Description

ID.2

Data type

boolean

syncope or equivocal stress testing including exercise ecg,
Description

ID.3

Data type

boolean

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

ID.4

Data type

boolean

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

ID.5

Data type

boolean

patient agrees to participate and signs the informed consent
Description

ID.6

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.7

Data type

boolean

contraindications to the administration of iodinated contrast,
Description

ID.8

Data type

boolean

pregnancy, acute coronary syndromes,
Description

ID.9

Data type

boolean

and ventricular and/or supraventricular arrhythmias.
Description

ID.10

Data type

boolean

Similar models

Eligibility Coronary Artery Disease NCT01562730

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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