ID

34163

Descrição

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

Palavras-chave

  1. 14/01/2019 14/01/2019 -
Titular dos direitos

see on clinicaltrials.gov

Transferido a

14 de janeiro de 2019

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0

Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Breast Cancer NCT02067884

Eligibility Breast Cancer NCT02067884

Inclusion Criteria
Descrição

Inclusion Criteria

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

ID.1

Tipo de dados

boolean

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

ID.2

Tipo de dados

boolean

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

ID.3

Tipo de dados

boolean

women competent to sign study specific written informed consent
Descrição

ID.4

Tipo de dados

boolean

women willing to comply with protocol requirements
Descrição

ID.5

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
women who are pregnant
Descrição

ID.6

Tipo de dados

boolean

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

ID.7

Tipo de dados

boolean

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

ID.8

Tipo de dados

boolean

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

ID.9

Tipo de dados

boolean

women who cannot consent for themselves
Descrição

ID.10

Tipo de dados

boolean

Similar models

Eligibility Breast Cancer NCT02067884

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial