ID

34096

Descripción

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

Link

https://clinicaltrials.gov/show/NCT00863382

Palabras clave

  1. 14/1/19 14/1/19 - Julian Varghese
  2. 14/5/19 14/5/19 -
Titular de derechos de autor

see ClinicalTrials.gov

Subido en

14 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Atrial Fibrillation NCT00863382

Eligibility Atrial Fibrillation NCT00863382

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.2

Tipo de datos

boolean

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

ID.3

Tipo de datos

boolean

subjects who are scheduled for radiation therapy
Descripción

ID.4

Tipo de datos

boolean

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

ID.5

Tipo de datos

boolean

subjects who are scheduled for mri
Descripción

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

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

ID.8

Tipo de datos

boolean

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

ID.9

Tipo de datos

boolean

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

ID.10

Tipo de datos

boolean

Similar models

Eligibility Atrial Fibrillation NCT00863382

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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