ID

16526

Beschrijving

Outcomes Following Myocardial Revascularization: On and Off Cardiopulmonary Bypass; ODM derived from: https://clinicaltrials.gov/show/NCT00032630

Link

https://clinicaltrials.gov/show/NCT00032630

Trefwoorden

  1. 22-07-16 22-07-16 -
Geüploaded op

22 juli 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Ischemic Heart Disease NCT00032630

Eligibility Ischemic Heart Disease NCT00032630

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
elective or urgent cabg
Beschrijving

cabg

Datatype

boolean

Alias
UMLS CUI [1]
C0010055
cabg only procedure to be performed
Beschrijving

cabg only procedure to be performed

Datatype

boolean

Alias
UMLS CUI [1]
C0393107
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient's surgeon is not a participant that meets study off-pup criteria
Beschrijving

ID.3

Datatype

boolean

valve or valve/cabg procedure
Beschrijving

valve or valve/cabg procedure

Datatype

boolean

Alias
UMLS CUI [1]
C1292963
UMLS CUI [2]
C0010055
emergent, hemodynamically unstable, or in cardiogenic shock preoperatively
Beschrijving

emergent

Datatype

boolean

Alias
UMLS CUI [1]
C0184893
moderate, moderate to severe, or severe valvular disease
Beschrijving

moderate to severe valvular disease

Datatype

boolean

Alias
UMLS CUI [1]
C3258293
enrolled in another therapeutic or interventional study
Beschrijving

clinical trial participation status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
majority of diffusely diseased distal vessels
Beschrijving

diffusely diseased distal vessels

Datatype

boolean

Alias
UMLS CUI [1]
C0085096
clinical care team has reservations
Beschrijving

clinical care team has reservations

Datatype

boolean

history of on-compliance
Beschrijving

compliance

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
patient preference for treatment arm
Beschrijving

patient preference for treatment arm

Datatype

boolean

inability to provide informed consent
Beschrijving

inability to provide informed consent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488

Similar models

Eligibility Ischemic Heart Disease NCT00032630

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
cabg
Item
elective or urgent cabg
boolean
C0010055 (UMLS CUI [1])
cabg only procedure to be performed
Item
cabg only procedure to be performed
boolean
C0393107 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.3
Item
patient's surgeon is not a participant that meets study off-pup criteria
boolean
valve or valve/cabg procedure
Item
valve or valve/cabg procedure
boolean
C1292963 (UMLS CUI [1])
C0010055 (UMLS CUI [2])
emergent
Item
emergent, hemodynamically unstable, or in cardiogenic shock preoperatively
boolean
C0184893 (UMLS CUI [1])
moderate to severe valvular disease
Item
moderate, moderate to severe, or severe valvular disease
boolean
C3258293 (UMLS CUI [1])
clinical trial participation status
Item
enrolled in another therapeutic or interventional study
boolean
C2348568 (UMLS CUI [1])
diffusely diseased distal vessels
Item
majority of diffusely diseased distal vessels
boolean
C0085096 (UMLS CUI [1])
clinical care team has reservations
Item
clinical care team has reservations
boolean
compliance
Item
history of on-compliance
boolean
C1321605 (UMLS CUI [1])
patient preference for treatment arm
Item
patient preference for treatment arm
boolean
inability to provide informed consent
Item
inability to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])

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