ID

34142

Description

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

Lien

https://clinicaltrials.gov/show/NCT02514876

Mots-clés

  1. 14/01/2019 14/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

14 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT02514876

Eligibility Atrial Fibrillation NCT02514876

Inclusion Criteria
Description

Inclusion Criteria

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

ID.1

Type de données

boolean

patient is undergoing an atrial fibrillation ablation procedure.
Description

ID.2

Type de données

boolean

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

ID.3

Type de données

boolean

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

ID.4

Type de données

boolean

Exclusion Criteria
Description

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).
Description

ID.5

Type de données

boolean

patients in whom transseptal puncture is relatively contraindicated.
Description

ID.6

Type de données

boolean

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

ID.7

Type de données

boolean

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

ID.8

Type de données

boolean

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

ID.9

Type de données

boolean

Similar models

Eligibility Atrial Fibrillation NCT02514876

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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