ID

34218

Descripción

Stress Testing Compared to Coronary Computed Tomographic Angiography in Patients With Suspected Coronary Artery Disease; ODM derived from: https://clinicaltrials.gov/show/NCT01368770

Link

https://clinicaltrials.gov/show/NCT01368770

Palabras clave

  1. 15/1/19 15/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

15 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT01368770

Eligibility Coronary Artery Disease NCT01368770

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
consenting patients above 21 years who are mildly symptomatic (those in class ii nyha), who have an intermediate likelihood of cad, or asymptomatic patients who are determined to be at intermediate or high risk of coronary events by the framingham (atp iii) criteria
Descripción

ID.1

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with prior documented cad (by angiography), mi, coronary stenting or bypass surgery
Descripción

ID.2

Tipo de datos

boolean

patients in class iii or iv nyha
Descripción

ID.3

Tipo de datos

boolean

patients with chronic renal impairment to the extent of precluding contrast injection
Descripción

ID.4

Tipo de datos

boolean

severe medical disease with limited expectancy of life
Descripción

ID.5

Tipo de datos

boolean

contra-indication or allergy to pharmacologic stress agents or contrast agents
Descripción

ID.6

Tipo de datos

boolean

patients with unstable cardiac rhythms (including persistent atrial fibrillation) which preclude good ecg gating
Descripción

ID.7

Tipo de datos

boolean

weight limitations due to scanner design
Descripción

ID.8

Tipo de datos

boolean

pregnant/ lactating women
Descripción

ID.9

Tipo de datos

boolean

Similar models

Eligibility Coronary Artery Disease NCT01368770

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
consenting patients above 21 years who are mildly symptomatic (those in class ii nyha), who have an intermediate likelihood of cad, or asymptomatic patients who are determined to be at intermediate or high risk of coronary events by the framingham (atp iii) criteria
boolean
Item Group
C0680251 (UMLS CUI)
ID.2
Item
patients with prior documented cad (by angiography), mi, coronary stenting or bypass surgery
boolean
ID.3
Item
patients in class iii or iv nyha
boolean
ID.4
Item
patients with chronic renal impairment to the extent of precluding contrast injection
boolean
ID.5
Item
severe medical disease with limited expectancy of life
boolean
ID.6
Item
contra-indication or allergy to pharmacologic stress agents or contrast agents
boolean
ID.7
Item
patients with unstable cardiac rhythms (including persistent atrial fibrillation) which preclude good ecg gating
boolean
ID.8
Item
weight limitations due to scanner design
boolean
ID.9
Item
pregnant/ lactating women
boolean

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