ID

34096

Beschrijving

Comparison of External Event Recorders for Atrial Fibrillation Monitoring; ODM derived from: https://clinicaltrials.gov/show/NCT00863382

Link

https://clinicaltrials.gov/show/NCT00863382

Trefwoorden

  1. 14-01-19 14-01-19 - Julian Varghese
  2. 14-05-19 14-05-19 -
Houder van rechten

see ClinicalTrials.gov

Geüploaded op

14 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Atrial Fibrillation NCT00863382

Eligibility Atrial Fibrillation NCT00863382

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
all subjects who undergo radiofrequency ablation of paroxysmal af.
Beschrijving

ID.1

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with known allergy to sticky patches of event monitor
Beschrijving

ID.2

Datatype

boolean

subjects with skin infection or other problems on the chest that interferes with monitor implantation
Beschrijving

ID.3

Datatype

boolean

subjects who are scheduled for radiation therapy
Beschrijving

ID.4

Datatype

boolean

subjects who are scheduled for therapeutic ultrasound (like lithotripsy)
Beschrijving

ID.5

Datatype

boolean

subjects who are scheduled for mri
Beschrijving

ID.6

Datatype

boolean

subjects who are scheduled for a procedure that uses diathermy.
Beschrijving

ID.7

Datatype

boolean

subjects, in the opinion of the investigator, are not suitable candidates for the study
Beschrijving

ID.8

Datatype

boolean

subjects that do not have analog telephone line at home.
Beschrijving

ID.9

Datatype

boolean

existing cardiac rhythm management device (e.g., pacemaker or icd)
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Atrial Fibrillation NCT00863382

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
all subjects who undergo radiofrequency ablation of paroxysmal af.
boolean
Item Group
C0680251 (UMLS CUI)
ID.2
Item
subjects with known allergy to sticky patches of event monitor
boolean
ID.3
Item
subjects with skin infection or other problems on the chest that interferes with monitor implantation
boolean
ID.4
Item
subjects who are scheduled for radiation therapy
boolean
ID.5
Item
subjects who are scheduled for therapeutic ultrasound (like lithotripsy)
boolean
ID.6
Item
subjects who are scheduled for mri
boolean
ID.7
Item
subjects who are scheduled for a procedure that uses diathermy.
boolean
ID.8
Item
subjects, in the opinion of the investigator, are not suitable candidates for the study
boolean
ID.9
Item
subjects that do not have analog telephone line at home.
boolean
ID.10
Item
existing cardiac rhythm management device (e.g., pacemaker or icd)
boolean

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