ID

34155

Description

Contrast-Enhanced Digital Mammography (CEDM) for Identifying a Change in Management of Women With Newly Diagnosed Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01303419

Link

https://clinicaltrials.gov/show/NCT01303419

Keywords

  1. 1/14/19 1/14/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 14, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01303419

Eligibility Breast Cancer NCT01303419

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
woman 21 years of age or older
Description

ID.1

Data type

boolean

the subject is able and willing to comply with study procedures and signed and dated informed consent is obtained.
Description

ID.2

Data type

boolean

newly diagnosed with breast cancer (dcis or invasive) identified through core biopsy or fine-needle aspiration (fna) within last 30 days.
Description

ID.3

Data type

boolean

will have or have had a bilateral ce-bmri performed within 30 days after the new breast cancer diagnosis.
Description

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
woman who has already had a lumpectomy for the index lesion.
Description

ID.5

Data type

boolean

woman undergoing neoadjuvant chemotherapy treatment, hormone treatment or radiation therapy.
Description

ID.6

Data type

boolean

woman who is pregnant or who believe she may be pregnant.
Description

ID.7

Data type

boolean

woman who has breast implant.
Description

ID.8

Data type

boolean

woman who has a contraindication to the intravenous use of iodinated or gadolinium-chelated contrast agent (e.g., allergy to either agent or severely impaired renal function).
Description

ID.9

Data type

boolean

Similar models

Eligibility Breast Cancer NCT01303419

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
woman 21 years of age or older
boolean
ID.2
Item
the subject is able and willing to comply with study procedures and signed and dated informed consent is obtained.
boolean
ID.3
Item
newly diagnosed with breast cancer (dcis or invasive) identified through core biopsy or fine-needle aspiration (fna) within last 30 days.
boolean
ID.4
Item
will have or have had a bilateral ce-bmri performed within 30 days after the new breast cancer diagnosis.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
woman who has already had a lumpectomy for the index lesion.
boolean
ID.6
Item
woman undergoing neoadjuvant chemotherapy treatment, hormone treatment or radiation therapy.
boolean
ID.7
Item
woman who is pregnant or who believe she may be pregnant.
boolean
ID.8
Item
woman who has breast implant.
boolean
ID.9
Item
woman who has a contraindication to the intravenous use of iodinated or gadolinium-chelated contrast agent (e.g., allergy to either agent or severely impaired renal function).
boolean

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