ID

34313

Descripción

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

Link

https://clinicaltrials.gov/show/NCT02190877

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

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Heart Failure NCT02190877

Eligibility Heart Failure NCT02190877

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 a current prescription for a diuretic medication.
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 NCT02190877

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 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

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial