ID

34313

Descrição

Monitoring Subjects With Fluid-Management Issues In the Home Environment; ODM derived from: https://clinicaltrials.gov/show/NCT02190877

Link

https://clinicaltrials.gov/show/NCT02190877

Palavras-chave

  1. 16/01/2019 16/01/2019 -
Titular dos direitos

see on clinicaltrials.gov

Transferido a

16 de janeiro de 2019

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Heart Failure NCT02190877

Eligibility Heart Failure NCT02190877

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject is between 21 (twenty-one) and 90 (ninety) years of age at screening.
Descrição

ID.1

Tipo de dados

boolean

subject will have a current prescription for a diuretic medication.
Descrição

ID.2

Tipo de dados

boolean

subject and/or legally authorized person/representative is willing to undergo the informed consent process prior to enrollment in the study.
Descrição

ID.3

Tipo de dados

boolean

subject is a candidate for this study based on the pi's opinion and knowledge of the subject's condition.
Descrição

ID.4

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject is participating in another clinical study that may affect the results of either study.
Descrição

ID.5

Tipo de dados

boolean

subject is unable or not willing to wear electrode patches as required.
Descrição

ID.6

Tipo de dados

boolean

subject has skin sensitivity to adhesive or hydrogel materials used in electrode patches.
Descrição

ID.7

Tipo de dados

boolean

subject has a pacemaker, implanted cardioverter-defibrillator, or ventricular assist device.
Descrição

ID.8

Tipo de dados

boolean

subject is considered by the pi to be medically unsuitable for study participation.
Descrição

ID.9

Tipo de dados

boolean

Similar models

Eligibility Heart Failure NCT02190877

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
subject is between 21 (twenty-one) and 90 (ninety) years of age at screening.
boolean
ID.2
Item
subject will have a current prescription for a diuretic medication.
boolean
ID.3
Item
subject and/or legally authorized person/representative is willing to undergo the informed consent process prior to enrollment in the study.
boolean
ID.4
Item
subject is a candidate for this study based on the pi's opinion and knowledge of the subject's condition.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
subject is participating in another clinical study that may affect the results of either study.
boolean
ID.6
Item
subject is unable or not willing to wear electrode patches as required.
boolean
ID.7
Item
subject has skin sensitivity to adhesive or hydrogel materials used in electrode patches.
boolean
ID.8
Item
subject has a pacemaker, implanted cardioverter-defibrillator, or ventricular assist device.
boolean
ID.9
Item
subject is considered by the pi to be medically unsuitable for study participation.
boolean

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