ID

34235

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02456467

Nyckelord

  1. 2019-01-15 2019-01-15 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

15 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT02456467

Eligibility Coronary Artery Disease NCT02456467

Inclusion Criteria
Beskrivning

Inclusion Criteria

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

ID.1

Datatyp

boolean

subject is older than 18 years
Beskrivning

ID.2

Datatyp

boolean

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

ID.3

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.4

Datatyp

boolean

subject is incarcerated at the time of the study
Beskrivning

ID.5

Datatyp

boolean

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

ID.6

Datatyp

boolean

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

ID.7

Datatyp

boolean

patients with history of active liver disease
Beskrivning

ID.8

Datatyp

boolean

patients on emergency cases
Beskrivning

ID.9

Datatyp

boolean

patients on heparin anticoagulation before the beginning of the study
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Coronary Artery Disease NCT02456467

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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