ID

34146

Description

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

Keywords

  1. 1/14/19 1/14/19 -
  2. 5/14/19 5/14/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 14, 2019

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Bradycardia NCT01922726

Eligibility Bradycardia NCT01922726

Inclusion Criteria
Description

Inclusion Criteria

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

ID.1

Data type

boolean

patient with reply 200 dr implantation performed
Description

ID.2

Data type

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)
Description

ID.3

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.4

Data type

boolean

unavailability for routine follow-ups at the implanting centre
Description

ID.5

Data type

boolean

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

ID.6

Data type

boolean

inability or refusal to provide informed consent
Description

ID.7

Data type

boolean

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

ID.8

Data type

boolean

patient is pregnant
Description

ID.9

Data type

boolean

patient is forfeiture of freedom or under guardianship
Description

ID.10

Data type

boolean

Similar models

Eligibility Bradycardia NCT01922726

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

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