ID

34139

Descripción

D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation of Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT02199080

Link

https://clinicaltrials.gov/show/NCT02199080

Palabras clave

  1. 14/1/19 14/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

14 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT02199080

Eligibility Atrial Fibrillation NCT02199080

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
age> 18 years.
Descripción

ID.1

Tipo de datos

boolean

patients hospitalized for ablation of atrial fibrillation or symptomatic left flutter
Descripción

ID.2

Tipo de datos

boolean

patient informed of the study
Descripción

ID.3

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
age <18 years.
Descripción

ID.4

Tipo de datos

boolean

patients under guardianship
Descripción

ID.5

Tipo de datos

boolean

pregnant woman
Descripción

ID.6

Tipo de datos

boolean

contraindication to transesophageal echocardiography
Descripción

ID.7

Tipo de datos

boolean

transesophageal echocardiography made in another center as the center of ablation
Descripción

ID.8

Tipo de datos

boolean

refusal of the patient to participate in the study
Descripción

ID.9

Tipo de datos

boolean

patient participating in another interventional study in which an intervention related to biomedical research is performed before the transesophageal echocardiography
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Atrial Fibrillation NCT02199080

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
age> 18 years.
boolean
ID.2
Item
patients hospitalized for ablation of atrial fibrillation or symptomatic left flutter
boolean
ID.3
Item
patient informed of the study
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
age <18 years.
boolean
ID.5
Item
patients under guardianship
boolean
ID.6
Item
pregnant woman
boolean
ID.7
Item
contraindication to transesophageal echocardiography
boolean
ID.8
Item
transesophageal echocardiography made in another center as the center of ablation
boolean
ID.9
Item
refusal of the patient to participate in the study
boolean
ID.10
Item
patient participating in another interventional study in which an intervention related to biomedical research is performed before the transesophageal echocardiography
boolean

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