ID

34142

Beschreibung

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

Link

https://clinicaltrials.gov/show/NCT02514876

Stichworte

  1. 14.01.19 14.01.19 -
Rechteinhaber

see on clinicaltrials.gov

Hochgeladen am

14. Januar 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT02514876

Eligibility Atrial Fibrillation NCT02514876

Inclusion Criteria
Beschreibung

Inclusion Criteria

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

ID.1

Datentyp

boolean

patient is undergoing an atrial fibrillation ablation procedure.
Beschreibung

ID.2

Datentyp

boolean

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

ID.3

Datentyp

boolean

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

ID.4

Datentyp

boolean

Exclusion Criteria
Beschreibung

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).
Beschreibung

ID.5

Datentyp

boolean

patients in whom transseptal puncture is relatively contraindicated.
Beschreibung

ID.6

Datentyp

boolean

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

ID.7

Datentyp

boolean

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

ID.8

Datentyp

boolean

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

ID.9

Datentyp

boolean

Ähnliche Modelle

Eligibility Atrial Fibrillation NCT02514876

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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