ID

34235

Descripción

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

Link

https://clinicaltrials.gov/show/NCT02456467

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 NCT02456467

Eligibility Coronary Artery Disease NCT02456467

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

subject is older than 18 years
Descripción

ID.2

Tipo de datos

boolean

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

ID.3

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.4

Tipo de datos

boolean

subject is incarcerated at the time of the study
Descripción

ID.5

Tipo de datos

boolean

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

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

patients with history of active liver disease
Descripción

ID.8

Tipo de datos

boolean

patients on emergency cases
Descripción

ID.9

Tipo de datos

boolean

patients on heparin anticoagulation before the beginning of the study
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Coronary Artery Disease NCT02456467

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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