ID

34417

Description

Non-isotope Based Imaging Modalities vs Technetium-99m Single-Photon Emission Computed Tomography(99mTcSPECT); ODM derived from: https://clinicaltrials.gov/show/NCT01972360

Link

https://clinicaltrials.gov/show/NCT01972360

Keywords

  1. 1/17/19 1/17/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 17, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Myocardial Ischemia NCT01972360

Eligibility Myocardial Ischemia NCT01972360

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
clinically indicated request for spect
Description

ID.1

Data type

boolean

ability to undergo at least one of three non-nuclear imaging tests; cmr, ct or stress echocardiography
Description

ID.2

Data type

boolean

history of recent symptoms suggestive of myocardial ischemia
Description

ID.3

Data type

boolean

high risk for ischemic cardiovascular events
Description

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
severely reduced systolic function (lv ejection fraction less than 35%)
Description

ID.5

Data type

boolean

recent (less than 3 days) acute coronary syndrome including acute myocardial infarction
Description

ID.6

Data type

boolean

contraindications to dipyridamole spect including : i)severe reactive airway disease; ii) less than 3 days post myocardial infarction - acute coronary syndrome (mi-acs); iii) high-grade atrioventricular block (av block); iv)allergy to dipyridamole or theophylline; v) caffeine within 12 hours; vi) theophylline use within 48 hours; vii) severe claustrophobia; or viii) women who may be pregnant
Description

ID.7

Data type

boolean

kidney dysfunction (i.e estimated glomerular filtration rate (egfr) less than 45)
Description

ID.8

Data type

boolean

use of investigational drug or device within 30 days of screening visit
Description

ID.9

Data type

boolean

Similar models

Eligibility Myocardial Ischemia NCT01972360

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
clinically indicated request for spect
boolean
ID.2
Item
ability to undergo at least one of three non-nuclear imaging tests; cmr, ct or stress echocardiography
boolean
ID.3
Item
history of recent symptoms suggestive of myocardial ischemia
boolean
ID.4
Item
high risk for ischemic cardiovascular events
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
severely reduced systolic function (lv ejection fraction less than 35%)
boolean
ID.6
Item
recent (less than 3 days) acute coronary syndrome including acute myocardial infarction
boolean
ID.7
Item
contraindications to dipyridamole spect including : i)severe reactive airway disease; ii) less than 3 days post myocardial infarction - acute coronary syndrome (mi-acs); iii) high-grade atrioventricular block (av block); iv)allergy to dipyridamole or theophylline; v) caffeine within 12 hours; vi) theophylline use within 48 hours; vii) severe claustrophobia; or viii) women who may be pregnant
boolean
ID.8
Item
kidney dysfunction (i.e estimated glomerular filtration rate (egfr) less than 45)
boolean
ID.9
Item
use of investigational drug or device within 30 days of screening visit
boolean

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