ID

34313

Description

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

Link

https://clinicaltrials.gov/show/NCT02190877

Keywords

  1. 1/16/19 1/16/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 16, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Heart Failure NCT02190877

Eligibility Heart Failure NCT02190877

Inclusion Criteria
Description

Inclusion Criteria

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

ID.1

Data type

boolean

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

ID.2

Data type

boolean

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

ID.3

Data type

boolean

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

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.5

Data type

boolean

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

ID.6

Data type

boolean

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

ID.7

Data type

boolean

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

ID.8

Data type

boolean

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

ID.9

Data type

boolean

Similar models

Eligibility Heart Failure NCT02190877

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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