ID

34160

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01881880

Nyckelord

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

see on clinicaltrials.gov

Uppladdad den

14 januari 2019

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Breast Cancer NCT01881880

Eligibility Breast Cancer NCT01881880

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
women at least 40 years old
Beskrivning

ID.1

Datatyp

boolean

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

ID.2

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.3

Datatyp

boolean

subjects who have breast implants
Beskrivning

ID.4

Datatyp

boolean

personal history of breast cancer
Beskrivning

ID.5

Datatyp

boolean

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

ID.6

Datatyp

boolean

subjects who are breast-feeding
Beskrivning

ID.7

Datatyp

boolean

subjects who are unable or unwilling to tolerate study constraints
Beskrivning

ID.8

Datatyp

boolean

subjects unable or unwilling to undergo informed consent
Beskrivning

ID.9

Datatyp

boolean

subject with no rights from the national health insurance programme
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Breast Cancer NCT01881880

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

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial