ID

34571

Descripción

Reducing Atrial Pacing Rate to Reduce Atrial Fibrillation in Patients With Sick Sinus Syndrome.; ODM derived from: https://clinicaltrials.gov/show/NCT02034526

Link

https://clinicaltrials.gov/show/NCT02034526

Palabras clave

  1. 19/1/19 19/1/19 -
Titular de derechos de autor

GSK group of companies

Subido en

19 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Sinus Node Disease NCT02034526

Eligibility Sinus Node Disease NCT02034526

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
sick sinus syndrome and indication for first-time implantation of a ddd pacemaker: symptomatic sinus pauses (>2 sec) or bradycardia with or without paroxysmal af.
Descripción

ID.1

Tipo de datos

boolean

age ≥18 years.
Descripción

ID.2

Tipo de datos

boolean

patient informed consent.
Descripción

ID.3

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
permanent or persisting (>7 days) af prior to implantation.
Descripción

ID.4

Tipo de datos

boolean

persisting symptomatic sinus bradycardia and/or chronotropic incompetence where ddd-pacing at a frequency of >40 bpm is indicated (verified with long term ecg monitoring).
Descripción

ID.5

Tipo de datos

boolean

persisting second or third degree av block.
Descripción

ID.6

Tipo de datos

boolean

life expectancy <2 years.
Descripción

ID.7

Tipo de datos

boolean

participation in another interventional research study.
Descripción

ID.8

Tipo de datos

boolean

indication for implantable cardioverter defibrillator (icd) or cardiac resynchronization therapy (crt).
Descripción

ID.9

Tipo de datos

boolean

pregnancy.
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Sinus Node Disease NCT02034526

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
sick sinus syndrome and indication for first-time implantation of a ddd pacemaker: symptomatic sinus pauses (>2 sec) or bradycardia with or without paroxysmal af.
boolean
ID.2
Item
age ≥18 years.
boolean
ID.3
Item
patient informed consent.
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
permanent or persisting (>7 days) af prior to implantation.
boolean
ID.5
Item
persisting symptomatic sinus bradycardia and/or chronotropic incompetence where ddd-pacing at a frequency of >40 bpm is indicated (verified with long term ecg monitoring).
boolean
ID.6
Item
persisting second or third degree av block.
boolean
ID.7
Item
life expectancy <2 years.
boolean
ID.8
Item
participation in another interventional research study.
boolean
ID.9
Item
indication for implantable cardioverter defibrillator (icd) or cardiac resynchronization therapy (crt).
boolean
ID.10
Item
pregnancy.
boolean

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