ID

34165

Beschrijving

Comparison of Contrast-enhanced Spectral Mammography (CESM) to MRI in Screening High Risk Women for Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02275871

Link

https://clinicaltrials.gov/show/NCT02275871

Trefwoorden

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

see on clinicaltrials.gov

Geüploaded op

14 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT02275871

Eligibility Breast Cancer NCT02275871

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
women
Beschrijving

ID.1

Datatype

boolean

age > or equal to 30 years
Beschrijving

ID.2

Datatype

boolean

high risk (>20% lifetime risk)
Beschrijving

ID.3

Datatype

boolean

has a bilateral mammogram within the last 7 months
Beschrijving

ID.4

Datatype

boolean

has had a same day high risk screening mri
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
participants who have a known allergy or contraindication to iodinated contrast.
Beschrijving

ID.6

Datatype

boolean

participants who have a known allergy to food or medications.
Beschrijving

ID.7

Datatype

boolean

participants who have renal insufficiency or failure.
Beschrijving

ID.8

Datatype

boolean

participants who are pregnant or breastfeeding.
Beschrijving

ID.9

Datatype

boolean

participants with a concurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia.
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Breast Cancer NCT02275871

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
women
boolean
ID.2
Item
age > or equal to 30 years
boolean
ID.3
Item
high risk (>20% lifetime risk)
boolean
ID.4
Item
has a bilateral mammogram within the last 7 months
boolean
ID.5
Item
has had a same day high risk screening mri
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
participants who have a known allergy or contraindication to iodinated contrast.
boolean
ID.7
Item
participants who have a known allergy to food or medications.
boolean
ID.8
Item
participants who have renal insufficiency or failure.
boolean
ID.9
Item
participants who are pregnant or breastfeeding.
boolean
ID.10
Item
participants with a concurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia.
boolean

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