ID

34312

Descripción

Neck-Worn Monitoring Sensor for - A Study for Monitoring Subjects With Fluid-Management Issues During Dialysis; ODM derived from: https://clinicaltrials.gov/show/NCT02140905

Link

https://clinicaltrials.gov/show/NCT02140905

Palabras clave

  1. 16/1/19 16/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

16 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Heart Failure NCT02140905

Eligibility Heart Failure NCT02140905

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

subject will have one or more of the following clinical diagnoses related to fluid-management issues: esrd, heart failure.
Descripción

ID.2

Tipo de datos

boolean

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

ID.3

Tipo de datos

boolean

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

ID.4

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.5

Tipo de datos

boolean

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

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

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

ID.8

Tipo de datos

boolean

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

ID.9

Tipo de datos

boolean

Similar models

Eligibility Heart Failure NCT02140905

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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 one or more of the following clinical diagnoses related to fluid-management issues: esrd, heart failure.
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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