ID

34160

Descripción

Value of Tomosynthesis in Breast Lesion Characterization and Breast Cancer Staging; ODM derived from: https://clinicaltrials.gov/show/NCT01881880

Link

https://clinicaltrials.gov/show/NCT01881880

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 Breast Cancer NCT01881880

Eligibility Breast Cancer NCT01881880

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
women at least 40 years old
Descripción

ID.1

Tipo de datos

boolean

subject with a new lesion recommended for biopsy, whatever the modality which detected the lesion (clinical examination, mammography, tomosynthesis, us, or mri)
Descripción

ID.2

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with brca mutation or at high genetic risk
Descripción

ID.3

Tipo de datos

boolean

subjects who have breast implants
Descripción

ID.4

Tipo de datos

boolean

personal history of breast cancer
Descripción

ID.5

Tipo de datos

boolean

subjects who are pregnant or who think they may be pregnant
Descripción

ID.6

Tipo de datos

boolean

subjects who are breast-feeding
Descripción

ID.7

Tipo de datos

boolean

subjects who are unable or unwilling to tolerate study constraints
Descripción

ID.8

Tipo de datos

boolean

subjects unable or unwilling to undergo informed consent
Descripción

ID.9

Tipo de datos

boolean

subject with no rights from the national health insurance programme
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Breast Cancer NCT01881880

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
women at least 40 years old
boolean
ID.2
Item
subject with a new lesion recommended for biopsy, whatever the modality which detected the lesion (clinical examination, mammography, tomosynthesis, us, or mri)
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
subjects with brca mutation or at high genetic risk
boolean
ID.4
Item
subjects who have breast implants
boolean
ID.5
Item
personal history of breast cancer
boolean
ID.6
Item
subjects who are pregnant or who think they may be pregnant
boolean
ID.7
Item
subjects who are breast-feeding
boolean
ID.8
Item
subjects who are unable or unwilling to tolerate study constraints
boolean
ID.9
Item
subjects unable or unwilling to undergo informed consent
boolean
ID.10
Item
subject with no rights from the national health insurance programme
boolean

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