ID

11987

Description

Integrated RF and B-mode Deformation Analysis for 4D Stress Echocardiography; ODM derived from: https://clinicaltrials.gov/show/NCT02327455

Link

https://clinicaltrials.gov/show/NCT02327455

Keywords

  1. 8/30/15 8/30/15 -
Copyright Holder

ODM derived from: https://clinicaltrials.gov/show/NCT02327455

Uploaded on

August 30, 2015

DOI

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License

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT02327455

Eligibility Coronary Artery Disease NCT02327455

Inclusion Criteria
Description

Inclusion Criteria

at least 18 years of age, referred for clinically indicated dobutamine rest/stress tte
Description

at least 18 years of age; age at least 18 years; age at least 18 years; aged at least 18 years; dobutamine; stress

Data type

boolean

Alias
UMLS CUI [1]
C0001779
provide written informed consent to participate in the study
Description

written informed consent to participate in the study; provide written informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
availability for repease rest/stress test within on week of clinically indicated study
Description

stress; study

Data type

boolean

Alias
UMLS CUI [1]
C2036171
Exclusion Criteria
Description

Exclusion Criteria

unable to give informed consent
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
unstable hemodynamics that would not allow for repease rest/stress dobutamine transthoracic imaging
Description

dobutamine; stress

Data type

boolean

Alias
UMLS CUI [1]
C0019010
recurrent life threatening arrhythmias
Description

life threatening; arrhythmias; recurrent

Data type

boolean

Alias
UMLS CUI [1]
C1517874
UMLS CUI [2]
C0003811
UMLS CUI [3]
C2945760
heart rate >110 bpm
Description

heart rate

Data type

boolean

Alias
UMLS CUI [1]
C0018810
inadequate windows for transthoracic imagine
Description

no code found

Data type

boolean

patients that have a narrow-angle glaucoma (contraindication for atropine)
Description

glaucoma

Data type

boolean

Alias
UMLS CUI [1]
C0017601
change in cardiac medications or management including, coronary revascularization beween intial and repeat tte study.
Description

medications; cardiac; study

Data type

boolean

Alias
UMLS CUI [1]
C0488501
UMLS CUI [2]
C1522601
UMLS CUI [3]
C0008976

Similar models

Eligibility Coronary Artery Disease NCT02327455

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
at least 18 years of age; age at least 18 years; age at least 18 years; aged at least 18 years; dobutamine; stress
Item
at least 18 years of age, referred for clinically indicated dobutamine rest/stress tte
boolean
C0001779 (UMLS CUI [1])
written informed consent to participate in the study; provide written informed consent
Item
provide written informed consent to participate in the study
boolean
C0021430 (UMLS CUI [1])
stress; study
Item
availability for repease rest/stress test within on week of clinically indicated study
boolean
C2036171 (UMLS CUI [1])
informed consent
Item
unable to give informed consent
boolean
C0021430 (UMLS CUI [1])
dobutamine; stress
Item
unstable hemodynamics that would not allow for repease rest/stress dobutamine transthoracic imaging
boolean
C0019010 (UMLS CUI [1])
life threatening; arrhythmias; recurrent
Item
recurrent life threatening arrhythmias
boolean
C1517874 (UMLS CUI [1])
C0003811 (UMLS CUI [2])
C2945760 (UMLS CUI [3])
heart rate
Item
heart rate >110 bpm
boolean
C0018810 (UMLS CUI [1])
no code found
Item
inadequate windows for transthoracic imagine
boolean
glaucoma
Item
patients that have a narrow-angle glaucoma (contraindication for atropine)
boolean
C0017601 (UMLS CUI [1])
medications; cardiac; study
Item
change in cardiac medications or management including, coronary revascularization beween intial and repeat tte study.
boolean
C0488501 (UMLS CUI [1])
C1522601 (UMLS CUI [2])
C0008976 (UMLS CUI [3])

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