ID

34313

Beschreibung

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

Link

https://clinicaltrials.gov/show/NCT02190877

Stichworte

  1. 16.01.19 16.01.19 -
Rechteinhaber

see on clinicaltrials.gov

Hochgeladen am

16. Januar 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Heart Failure NCT02190877

Eligibility Heart Failure NCT02190877

Inclusion Criteria
Beschreibung

Inclusion Criteria

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

ID.1

Datentyp

boolean

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

ID.2

Datentyp

boolean

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

ID.3

Datentyp

boolean

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

ID.4

Datentyp

boolean

Exclusion Criteria
Beschreibung

Exclusion Criteria

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

ID.5

Datentyp

boolean

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

ID.6

Datentyp

boolean

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

ID.7

Datentyp

boolean

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

ID.8

Datentyp

boolean

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

ID.9

Datentyp

boolean

Ähnliche Modelle

Eligibility Heart Failure NCT02190877

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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