Information:
Fel:
ID
34163
Beskrivning
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
Länk
https://clinicaltrials.gov/show/NCT02067884
Nyckelord
Versioner (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 NCT02067884
Eligibility Breast Cancer NCT02067884
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT02067884
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
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
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