ID

34132

Description

Video-Assisted Thoracoscopic Pulmonary Vein Isolation Versus Percutaneous Catheter Ablation in Atrial Fibrillation Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01319747

Link

https://clinicaltrials.gov/show/NCT01319747

Keywords

  1. 1/14/19 1/14/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 14, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT01319747

Eligibility Atrial Fibrillation NCT01319747

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients > 18 years of age
Description

ID.1

Data type

boolean

documented, symptomatic, episodes of paroxysmal or persistent af
Description

ID.2

Data type

boolean

during the last 6 months patients must have at least 2 documented episodes of af, despite the use of at least 1 anti arrhythmic drug.
Description

ID.3

Data type

boolean

able of providing informed consent
Description

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy
Description

ID.5

Data type

boolean

unwillingness to use or contra-indications for vitamin k antagonists
Description

ID.6

Data type

boolean

severely enlarged left atrium (>50 mm) on echocardiography
Description

ID.7

Data type

boolean

prior af ablation or af surgery
Description

ID.8

Data type

boolean

intracardiac thrombus
Description

ID.9

Data type

boolean

prior heart surgery or pulmonary disease hampering thoracoscopic surgery
Description

ID.10

Data type

boolean

Similar models

Eligibility Atrial Fibrillation NCT01319747

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients > 18 years of age
boolean
ID.2
Item
documented, symptomatic, episodes of paroxysmal or persistent af
boolean
ID.3
Item
during the last 6 months patients must have at least 2 documented episodes of af, despite the use of at least 1 anti arrhythmic drug.
boolean
ID.4
Item
able of providing informed consent
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
pregnancy
boolean
ID.6
Item
unwillingness to use or contra-indications for vitamin k antagonists
boolean
ID.7
Item
severely enlarged left atrium (>50 mm) on echocardiography
boolean
ID.8
Item
prior af ablation or af surgery
boolean
ID.9
Item
intracardiac thrombus
boolean
ID.10
Item
prior heart surgery or pulmonary disease hampering thoracoscopic surgery
boolean

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