ID

34142

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02514876

Nyckelord

  1. 2019-01-14 2019-01-14 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

14 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT02514876

Eligibility Atrial Fibrillation NCT02514876

Inclusion Criteria
Beskrivning

Inclusion Criteria

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

ID.1

Datatyp

boolean

patient is undergoing an atrial fibrillation ablation procedure.
Beskrivning

ID.2

Datatyp

boolean

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

ID.3

Datatyp

boolean

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

ID.4

Datatyp

boolean

Exclusion Criteria
Beskrivning

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).
Beskrivning

ID.5

Datatyp

boolean

patients in whom transseptal puncture is relatively contraindicated.
Beskrivning

ID.6

Datatyp

boolean

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

ID.7

Datatyp

boolean

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

ID.8

Datatyp

boolean

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

ID.9

Datatyp

boolean

Similar models

Eligibility Atrial Fibrillation NCT02514876

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