ID

33592

Beschrijving

Non-Invasive Cardiac Output Measurement for CRT Optimization; ODM derived from: https://clinicaltrials.gov/show/NCT02126241

Link

https://clinicaltrials.gov/show/NCT02126241

Trefwoorden

  1. 14-12-18 14-12-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

14 december 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Congestive Heart Failure NCT02126241

Eligibility Congestive Heart Failure NCT02126241

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients implanted with a crt device at least 6 months before, in concordance with aha/acc or esc/ehra guidelines (class i or ii) for crt implantation
Beschrijving

Cardiac Resynchronization Therapy Device Implanted

Datatype

boolean

Alias
UMLS CUI [1,1]
C2936377
UMLS CUI [1,2]
C0021102
nyha class i - iii heart failure
Beschrijving

Heart failure New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
stable sinus rhythm
Beschrijving

Sinus rhythm Stable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0232201
UMLS CUI [1,2]
C0205360
bi-ventricular pacing ≥ 90%
Beschrijving

Biventricular Pacing Percentage

Datatype

boolean

Alias
UMLS CUI [1,1]
C2936372
UMLS CUI [1,2]
C0439165
patient provides informed consent.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
nyha class iv heart failure
Beschrijving

Heart failure New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
permanent or persistent atrial fibrillation
Beschrijving

Permanent atrial fibrillation | Persistent atrial fibrillation

Datatype

boolean

Alias
UMLS CUI [1]
C2586056
UMLS CUI [2]
C2585653
bi-ventricular pacing <90%
Beschrijving

Biventricular Pacing Percentage

Datatype

boolean

Alias
UMLS CUI [1,1]
C2936372
UMLS CUI [1,2]
C0439165
inability to perform the six-minute walk test
Beschrijving

6-Minute Walk Test Unable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0430515
UMLS CUI [1,2]
C1299582

Similar models

Eligibility Congestive Heart Failure NCT02126241

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Cardiac Resynchronization Therapy Device Implanted
Item
patients implanted with a crt device at least 6 months before, in concordance with aha/acc or esc/ehra guidelines (class i or ii) for crt implantation
boolean
C2936377 (UMLS CUI [1,1])
C0021102 (UMLS CUI [1,2])
Heart failure New York Heart Association Classification
Item
nyha class i - iii heart failure
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Sinus rhythm Stable
Item
stable sinus rhythm
boolean
C0232201 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Biventricular Pacing Percentage
Item
bi-ventricular pacing ≥ 90%
boolean
C2936372 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
Informed Consent
Item
patient provides informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Heart failure New York Heart Association Classification
Item
nyha class iv heart failure
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Permanent atrial fibrillation | Persistent atrial fibrillation
Item
permanent or persistent atrial fibrillation
boolean
C2586056 (UMLS CUI [1])
C2585653 (UMLS CUI [2])
Biventricular Pacing Percentage
Item
bi-ventricular pacing <90%
boolean
C2936372 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
6-Minute Walk Test Unable
Item
inability to perform the six-minute walk test
boolean
C0430515 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])

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