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ID
34096
Description
Comparison of External Event Recorders for Atrial Fibrillation Monitoring; ODM derived from: https://clinicaltrials.gov/show/NCT00863382
Link
https://clinicaltrials.gov/show/NCT00863382
Keywords
Versions (2)
- 1/14/19 1/14/19 - Julian Varghese
- 5/14/19 5/14/19 -
Copyright Holder
see ClinicalTrials.gov
Uploaded on
January 14, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Eligibility Atrial Fibrillation NCT00863382
Eligibility Atrial Fibrillation NCT00863382
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT00863382
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
ID.1
Item
all subjects who undergo radiofrequency ablation of paroxysmal af.
boolean
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