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Information:
Fel:
ID
34096
Beskrivning
Comparison of External Event Recorders for Atrial Fibrillation Monitoring; ODM derived from: https://clinicaltrials.gov/show/NCT00863382
Länk
https://clinicaltrials.gov/show/NCT00863382
Nyckelord
Versioner (2)
- 2019-01-14 2019-01-14 - Julian Varghese
- 2019-05-14 2019-05-14 -
Rättsinnehavare
see ClinicalTrials.gov
Uppladdad den
14 januari 2019
DOI
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Licens
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
Typ
Description | Question | Decode (Coded Value)
Datatyp
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