ID

34218

Description

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

Lien

https://clinicaltrials.gov/show/NCT01368770

Mots-clés

  1. 15/01/2019 15/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

15 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Coronary Artery Disease NCT01368770

Eligibility Coronary Artery Disease NCT01368770

Inclusion Criteria
Description

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
Description

ID.1

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.2

Type de données

boolean

patients in class iii or iv nyha
Description

ID.3

Type de données

boolean

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

ID.4

Type de données

boolean

severe medical disease with limited expectancy of life
Description

ID.5

Type de données

boolean

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

ID.6

Type de données

boolean

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

ID.7

Type de données

boolean

weight limitations due to scanner design
Description

ID.8

Type de données

boolean

pregnant/ lactating women
Description

ID.9

Type de données

boolean

Similar models

Eligibility Coronary Artery Disease NCT01368770

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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