ID

34163

Description

Contrast Enhanced Ultrasound and Shear Wave Elastography in Measuring Response in Patients With Breast Cancer Receiving Chemotherapy Before Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT02067884

Link

https://clinicaltrials.gov/show/NCT02067884

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 NCT02067884

Eligibility Breast Cancer NCT02067884

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
women with histologically confirmed breast cancer (by core needle biopsy)
Description

ID.1

Data type

boolean

women with >= 2 cm clinically or radiologically measureable breast cancer
Description

ID.2

Data type

boolean

women scheduled to receive neoadjuvant chemotherapy as part of their treatment plan
Description

ID.3

Data type

boolean

women competent to sign study specific written informed consent
Description

ID.4

Data type

boolean

women willing to comply with protocol requirements
Description

ID.5

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
women who are pregnant
Description

ID.6

Data type

boolean

women who have undergone open surgical (excisional) biopsy for breast cancer diagnosis
Description

ID.7

Data type

boolean

women who have had a prior history of breast cancer in the same breast
Description

ID.8

Data type

boolean

women with known cardiac shunt, pulmonary hypertension or hypersensitivity to perflutren agent
Description

ID.9

Data type

boolean

women who cannot consent for themselves
Description

ID.10

Data type

boolean

Similar models

Eligibility Breast Cancer NCT02067884

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
women with histologically confirmed breast cancer (by core needle biopsy)
boolean
ID.2
Item
women with >= 2 cm clinically or radiologically measureable breast cancer
boolean
ID.3
Item
women scheduled to receive neoadjuvant chemotherapy as part of their treatment plan
boolean
ID.4
Item
women competent to sign study specific written informed consent
boolean
ID.5
Item
women willing to comply with protocol requirements
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
women who are pregnant
boolean
ID.7
Item
women who have undergone open surgical (excisional) biopsy for breast cancer diagnosis
boolean
ID.8
Item
women who have had a prior history of breast cancer in the same breast
boolean
ID.9
Item
women with known cardiac shunt, pulmonary hypertension or hypersensitivity to perflutren agent
boolean
ID.10
Item
women who cannot consent for themselves
boolean

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