Informações:
Falhas:
ID
12430
Descrição
Breast VCEUS to Evaluate Early Response to Neoadjuvant Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT01817374
Link
https://clinicaltrials.gov/show/NCT01817374
Palavras-chave
Versões (2)
- 17/11/2015 17/11/2015 -
- 17/11/2015 17/11/2015 - Julian Varghese
Transferido a
17 de novembro de 2015
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT01817374
Eligibility Breast Cancer NCT01817374
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT01817374
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
age
Item
1. adult patients (age 19 years or older).
boolean
C0001779 (UMLS CUI [1])
Patients with newly diagnosed and untreated stage ii and iii breast cancer
Item
2. patients with newly diagnosed and untreated stage ii and iii breast cancer scheduled to undergo neoadjuvant chemotherapy.
boolean
C0006142 (UMLS CUI [1])
Informed consent
Item
3. patients with signed informed consent.
boolean
C0021430 (UMLS CUI [1])
Any history of prior radiation or chemotherapy for breast cancer
Item
1. any history of prior radiation or chemotherapy for breast cancer.
boolean
C1300985 (UMLS CUI [1])
Patients who only have non-measurable disease
Item
2. patients who only have non-measurable disease.
boolean
C3538912 (UMLS CUI [1])
Patients who are medically unstable
Item
3. patients who are medically unstable.
boolean
C3841317 (UMLS CUI [1])
Primary malignant neoplasm
Item
4. patients with other primary cancers requiring systemic treatment.
boolean
C1306459 (UMLS CUI [1])
Cardiac shunt
Item
5. patients with cardiac shunts.
boolean
C0232180 (UMLS CUI [1])
Patients with unstable cardiopulmonary conditions
Item
6. patients with unstable cardiopulmonary conditions.
boolean
C0238074 (UMLS CUI [1])
Pulmonary Hypertension
Item
7. patients with known pulmonary hypertension.
boolean
C0020542 (UMLS CUI [1])
Patients with known hypersensitivity
Item
8. patients with known hypersensitivity to any component of definity (r) microbubble contrast.
boolean
C0020517 (UMLS CUI [1])
pregnant and breast feeding
Item
9. patients who are pregnant, breast-feeding or are planning to become pregnant during the study duration.
boolean
C0006147 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0032961 (UMLS CUI [2])