ID

34235

Description

HemoSonics-UVA HemoSonics-UVA Cardiac Surgery Clinical Study Protocol; ODM derived from: https://clinicaltrials.gov/show/NCT02456467

Lien

https://clinicaltrials.gov/show/NCT02456467

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

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Eligibility Coronary Artery Disease NCT02456467

Eligibility Coronary Artery Disease NCT02456467

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject is scheduled for cardiac surgery involving bypass circuit
Description

ID.1

Type de données

boolean

subject is older than 18 years
Description

ID.2

Type de données

boolean

subject is willing to participate and he/she has signed a consent form
Description

ID.3

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject is unable to provide written informed consent
Description

ID.4

Type de données

boolean

subject is incarcerated at the time of the study
Description

ID.5

Type de données

boolean

subject is affected by any condition that, in the opinion of the surgical team, may pose additional risks
Description

ID.6

Type de données

boolean

patients with renal disease (defined as serum creatinine greater than 1.5 mg/dl)
Description

ID.7

Type de données

boolean

patients with history of active liver disease
Description

ID.8

Type de données

boolean

patients on emergency cases
Description

ID.9

Type de données

boolean

patients on heparin anticoagulation before the beginning of the study
Description

ID.10

Type de données

boolean

Similar models

Eligibility Coronary Artery Disease NCT02456467

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
subject is scheduled for cardiac surgery involving bypass circuit
boolean
ID.2
Item
subject is older than 18 years
boolean
ID.3
Item
subject is willing to participate and he/she has signed a consent form
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
subject is unable to provide written informed consent
boolean
ID.5
Item
subject is incarcerated at the time of the study
boolean
ID.6
Item
subject is affected by any condition that, in the opinion of the surgical team, may pose additional risks
boolean
ID.7
Item
patients with renal disease (defined as serum creatinine greater than 1.5 mg/dl)
boolean
ID.8
Item
patients with history of active liver disease
boolean
ID.9
Item
patients on emergency cases
boolean
ID.10
Item
patients on heparin anticoagulation before the beginning of the study
boolean

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