ID

34912

Beschrijving

Evaluation of a Novel Infra-red Breast Imaging System for Risk Assessment in Women at High Risk for Breast Cancer.; ODM derived from: https://clinicaltrials.gov/show/NCT02009150

Link

https://clinicaltrials.gov/show/NCT02009150

Trefwoorden

Versies (1)
  1. 04-02-19 04-02-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

4 februari 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.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

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

Eligibility Breast Cancer NCT02009150

Engels

Eligibility Breast Cancer NCT02009150

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
female
Beschrijving

Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
woman has read, understood and signed the inform consent form
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
age: 20 years and older
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
women who are asymptomatic for breast cancer
Beschrijving

Breast Carcinoma Asymptomatic

Datatype

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0231221
proven carriers of deleterious brca1 or brca2 mutations or women that were found to have a lifetime risk of developing breast cancer greater or equal to 20% based on gail or clause risk models
Beschrijving

Deleterious BRCA1 Gene Mutation | Deleterious BRCA2 Gene Mutation | Lifetime Risk Percentage Breast Carcinoma Gail model | Lifetime Risk Percentage Breast Carcinoma Claus Model

Datatype

boolean

Alias
UMLS CUI [1]
C4289700
UMLS CUI [2]
C4287905
UMLS CUI [3,1]
C1517878
UMLS CUI [3,2]
C0439165
UMLS CUI [3,3]
C0678222
UMLS CUI [3,4]
C1511297
UMLS CUI [4,1]
C1517878
UMLS CUI [4,2]
C0439165
UMLS CUI [4,3]
C0678222
UMLS CUI [4,4]
C1707405
women scheduled to undergo routine mammography and/or us or mri screening
Beschrijving

Routine Mammography Scheduled | Ultrasonography Scheduled | MRI Scheduled

Datatype

boolean

Alias
UMLS CUI [1,1]
C0205547
UMLS CUI [1,2]
C0024671
UMLS CUI [1,3]
C0205539
UMLS CUI [2,1]
C0041618
UMLS CUI [2,2]
C0205539
UMLS CUI [3,1]
C0024485
UMLS CUI [3,2]
C0205539
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
women who have had a mammography and/or ultrasound examination performed on the day of the study prior to mira scan
Beschrijving

Mammography | Ultrasonography | Other Coding

Datatype

boolean

Alias
UMLS CUI [1]
C0024671
UMLS CUI [2]
C0041618
UMLS CUI [3]
C3846158
women who had a lumpectomy surgery up to 5 years preceding the study
Beschrijving

Segmental Mastectomy

Datatype

boolean

Alias
UMLS CUI [1]
C0024885
women who had undergone mastectomy and/or reconstruction
Beschrijving

Mastectomy | Mammaplasty

Datatype

boolean

Alias
UMLS CUI [1]
C0024881
UMLS CUI [2]
C0085076
women who have undergone any type of breast surgery throughout the 6 months preceding the study
Beschrijving

Operation on breast Type Any

Datatype

boolean

Alias
UMLS CUI [1,1]
C3714726
UMLS CUI [1,2]
C0332307
UMLS CUI [1,3]
C1552551
women who have had a breast biopsy performed throughout the 6 weeks preceding the study.
Beschrijving

Biopsy of breast

Datatype

boolean

Alias
UMLS CUI [1]
C0405352
women who have a fever on the day of the mira imaging
Beschrijving

Fever | Other Coding

Datatype

boolean

Alias
UMLS CUI [1]
C0015967
UMLS CUI [2]
C3846158
women who are pregnant
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
women who are breast-feeding
Beschrijving

Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0006147
women who had undergone breast reduction/augmentation
Beschrijving

Reduction mammaplasty | Augmentation mammoplasty

Datatype

boolean

Alias
UMLS CUI [1]
C0191922
UMLS CUI [2]
C0191925
Terug naar het begin van de pagina

Similar models

Eligibility Breast Cancer NCT02009150

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Informed Consent
Item
woman has read, understood and signed the inform consent form
boolean
C0021430 (UMLS CUI [1])
Age
Item
age: 20 years and older
boolean
C0001779 (UMLS CUI [1])
Breast Carcinoma Asymptomatic
Item
women who are asymptomatic for breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0231221 (UMLS CUI [1,2])
Deleterious BRCA1 Gene Mutation | Deleterious BRCA2 Gene Mutation | Lifetime Risk Percentage Breast Carcinoma Gail model | Lifetime Risk Percentage Breast Carcinoma Claus Model
Item
proven carriers of deleterious brca1 or brca2 mutations or women that were found to have a lifetime risk of developing breast cancer greater or equal to 20% based on gail or clause risk models
boolean
C4289700 (UMLS CUI [1])
C4287905 (UMLS CUI [2])
C1517878 (UMLS CUI [3,1])
C0439165 (UMLS CUI [3,2])
C0678222 (UMLS CUI [3,3])
C1511297 (UMLS CUI [3,4])
C1517878 (UMLS CUI [4,1])
C0439165 (UMLS CUI [4,2])
C0678222 (UMLS CUI [4,3])
C1707405 (UMLS CUI [4,4])
Routine Mammography Scheduled | Ultrasonography Scheduled | MRI Scheduled
Item
women scheduled to undergo routine mammography and/or us or mri screening
boolean
C0205547 (UMLS CUI [1,1])
C0024671 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C0041618 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
C0024485 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Mammography | Ultrasonography | Other Coding
Item
women who have had a mammography and/or ultrasound examination performed on the day of the study prior to mira scan
boolean
C0024671 (UMLS CUI [1])
C0041618 (UMLS CUI [2])
C3846158 (UMLS CUI [3])
Segmental Mastectomy
Item
women who had a lumpectomy surgery up to 5 years preceding the study
boolean
C0024885 (UMLS CUI [1])
Mastectomy | Mammaplasty
Item
women who had undergone mastectomy and/or reconstruction
boolean
C0024881 (UMLS CUI [1])
C0085076 (UMLS CUI [2])
Operation on breast Type Any
Item
women who have undergone any type of breast surgery throughout the 6 months preceding the study
boolean
C3714726 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C1552551 (UMLS CUI [1,3])
Biopsy of breast
Item
women who have had a breast biopsy performed throughout the 6 weeks preceding the study.
boolean
C0405352 (UMLS CUI [1])
Fever | Other Coding
Item
women who have a fever on the day of the mira imaging
boolean
C0015967 (UMLS CUI [1])
C3846158 (UMLS CUI [2])
Pregnancy
Item
women who are pregnant
boolean
C0032961 (UMLS CUI [1])
Breast Feeding
Item
women who are breast-feeding
boolean
C0006147 (UMLS CUI [1])
Reduction mammaplasty | Augmentation mammoplasty
Item
women who had undergone breast reduction/augmentation
boolean
C0191922 (UMLS CUI [1])
C0191925 (UMLS CUI [2])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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