ID

34146

Descripción

Registry of Sleep Apnea Monitoring and Atrial Fibrillation in Pacemaker Patients (RESPIRE); ODM derived from: https://clinicaltrials.gov/show/NCT01922726

Link

https://clinicaltrials.gov/show/NCT01922726

Palabras clave

  1. 14/1/19 14/1/19 -
  2. 14/5/19 14/5/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

14 de enero de 2019

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0

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 Bradycardia NCT01922726

Eligibility Bradycardia NCT01922726

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient eligible for implantation of a dual-chamber pacemaker according to current available guidelines
Descripción

ID.1

Tipo de datos

boolean

patient with reply 200 dr implantation performed
Descripción

ID.2

Tipo de datos

boolean

patient who provides signed and dated informed consent (according to the laws and regulations of the country in which the observational study is conducted)
Descripción

ID.3

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
inability to understand the purpose of the study or refusal to co-operate
Descripción

ID.4

Tipo de datos

boolean

unavailability for routine follow-ups at the implanting centre
Descripción

ID.5

Tipo de datos

boolean

already included in another clinical study that could affect the results of this study
Descripción

ID.6

Tipo de datos

boolean

inability or refusal to provide informed consent
Descripción

ID.7

Tipo de datos

boolean

patient is minor (less than 18-years old)
Descripción

ID.8

Tipo de datos

boolean

patient is pregnant
Descripción

ID.9

Tipo de datos

boolean

patient is forfeiture of freedom or under guardianship
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Bradycardia NCT01922726

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patient eligible for implantation of a dual-chamber pacemaker according to current available guidelines
boolean
ID.2
Item
patient with reply 200 dr implantation performed
boolean
ID.3
Item
patient who provides signed and dated informed consent (according to the laws and regulations of the country in which the observational study is conducted)
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
inability to understand the purpose of the study or refusal to co-operate
boolean
ID.5
Item
unavailability for routine follow-ups at the implanting centre
boolean
ID.6
Item
already included in another clinical study that could affect the results of this study
boolean
ID.7
Item
inability or refusal to provide informed consent
boolean
ID.8
Item
patient is minor (less than 18-years old)
boolean
ID.9
Item
patient is pregnant
boolean
ID.10
Item
patient is forfeiture of freedom or under guardianship
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