ID

34165

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02275871

Nyckelord

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

see on clinicaltrials.gov

Uppladdad den

14 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT02275871

Eligibility Breast Cancer NCT02275871

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
women
Beskrivning

ID.1

Datatyp

boolean

age > or equal to 30 years
Beskrivning

ID.2

Datatyp

boolean

high risk (>20% lifetime risk)
Beskrivning

ID.3

Datatyp

boolean

has a bilateral mammogram within the last 7 months
Beskrivning

ID.4

Datatyp

boolean

has had a same day high risk screening mri
Beskrivning

ID.5

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.6

Datatyp

boolean

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

ID.7

Datatyp

boolean

participants who have renal insufficiency or failure.
Beskrivning

ID.8

Datatyp

boolean

participants who are pregnant or breastfeeding.
Beskrivning

ID.9

Datatyp

boolean

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

ID.10

Datatyp

boolean

Similar models

Eligibility Breast Cancer NCT02275871

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