ID

34571

Beschrijving

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

Trefwoorden

  1. 19-01-19 19-01-19 -
Houder van rechten

GSK group of companies

Geüploaded op

19 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Sinus Node Disease NCT02034526

Eligibility Sinus Node Disease NCT02034526

Inclusion Criteria
Beschrijving

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.
Beschrijving

ID.1

Datatype

boolean

age ≥18 years.
Beschrijving

ID.2

Datatype

boolean

patient informed consent.
Beschrijving

ID.3

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

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

ID.4

Datatype

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).
Beschrijving

ID.5

Datatype

boolean

persisting second or third degree av block.
Beschrijving

ID.6

Datatype

boolean

life expectancy <2 years.
Beschrijving

ID.7

Datatype

boolean

participation in another interventional research study.
Beschrijving

ID.8

Datatype

boolean

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

ID.9

Datatype

boolean

pregnancy.
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Sinus Node Disease NCT02034526

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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