ID

34142

Descrição

Colibri Foresight ICE System; ODM derived from: https://clinicaltrials.gov/show/NCT02514876

Link

https://clinicaltrials.gov/show/NCT02514876

Palavras-chave

  1. 14/01/2019 14/01/2019 -
Titular dos direitos

see on clinicaltrials.gov

Transferido a

14 de janeiro de 2019

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT02514876

Eligibility Atrial Fibrillation NCT02514876

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient is at least 18 years old.
Descrição

ID.1

Tipo de dados

boolean

patient is undergoing an atrial fibrillation ablation procedure.
Descrição

ID.2

Tipo de dados

boolean

patient has a transesophageal echocardiogram (tee) within the 48 hours prior to ablation procedure to rule out left atrial thrombus.
Descrição

ID.3

Tipo de dados

boolean

patient provides informed, written consent for participation in the study.
Descrição

ID.4

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients in whom placement of an ice catheter in the right atrium for adequate atrial visualization is not technically feasible (as evaluated and determined by the physician performing the procedure).
Descrição

ID.5

Tipo de dados

boolean

patients in whom transseptal puncture is relatively contraindicated.
Descrição

ID.6

Tipo de dados

boolean

patients in whom left atrial clot or dense spontaneous contrast is identified on tee, which would increase thromboembolic risk.
Descrição

ID.7

Tipo de dados

boolean

women of child bearing potential, in whom pregnancy cannot be excluded.
Descrição

ID.8

Tipo de dados

boolean

patients unable to grant informed, written consent for participation in the study.
Descrição

ID.9

Tipo de dados

boolean

Similar models

Eligibility Atrial Fibrillation NCT02514876

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patient is at least 18 years old.
boolean
ID.2
Item
patient is undergoing an atrial fibrillation ablation procedure.
boolean
ID.3
Item
patient has a transesophageal echocardiogram (tee) within the 48 hours prior to ablation procedure to rule out left atrial thrombus.
boolean
ID.4
Item
patient provides informed, written consent for participation in the study.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
patients in whom placement of an ice catheter in the right atrium for adequate atrial visualization is not technically feasible (as evaluated and determined by the physician performing the procedure).
boolean
ID.6
Item
patients in whom transseptal puncture is relatively contraindicated.
boolean
ID.7
Item
patients in whom left atrial clot or dense spontaneous contrast is identified on tee, which would increase thromboembolic risk.
boolean
ID.8
Item
women of child bearing potential, in whom pregnancy cannot be excluded.
boolean
ID.9
Item
patients unable to grant informed, written consent for participation in the study.
boolean

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