ID

34160

Beschrijving

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

Trefwoorden

  1. 14-01-19 14-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

14 januari 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Breast Cancer NCT01881880

Eligibility Breast Cancer NCT01881880

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
women at least 40 years old
Beschrijving

ID.1

Datatype

boolean

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

ID.2

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

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

ID.3

Datatype

boolean

subjects who have breast implants
Beschrijving

ID.4

Datatype

boolean

personal history of breast cancer
Beschrijving

ID.5

Datatype

boolean

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

ID.6

Datatype

boolean

subjects who are breast-feeding
Beschrijving

ID.7

Datatype

boolean

subjects who are unable or unwilling to tolerate study constraints
Beschrijving

ID.8

Datatype

boolean

subjects unable or unwilling to undergo informed consent
Beschrijving

ID.9

Datatype

boolean

subject with no rights from the national health insurance programme
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Breast Cancer NCT01881880

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

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