ID

12415

Descripción

Breast VCEUS to Evaluate Early Response to Neoadjuvant Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT01817374

Link

https://clinicaltrials.gov/show/NCT01817374

Palabras clave

  1. 17/11/15 17/11/15 -
  2. 17/11/15 17/11/15 - Julian Varghese
Subido en

17 de noviembre de 2015

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Breast Cancer NCT01817374

Eligibility Breast Cancer NCT01817374

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. adult patients (age 19 years or older).
Descripción

Adult patients

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0030705
2. patients with newly diagnosed and untreated stage ii and iii breast cancer scheduled to undergo neoadjuvant chemotherapy.
Descripción

Patients with newly diagnosed and untreated stage ii and iii breast cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006142
3. patients with signed informed consent.
Descripción

Informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0514044
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. any history of prior radiation or chemotherapy for breast cancer.
Descripción

Any history of prior radiation or chemotherapy for breast cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1300985
2. patients who only have non-measurable disease.
Descripción

Patients who only have non-measurable disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3538912
3. patients who are medically unstable.
Descripción

Patients who are medically unstable

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3841317
4. patients with other primary cancers requiring systemic treatment.
Descripción

Primary malignant neoplasm

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1306459
5. patients with cardiac shunts.
Descripción

Cardiac shunt

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232180
6. patients with unstable cardiopulmonary conditions.
Descripción

Patients with unstable cardiopulmonary conditions

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0238074
7. patients with known pulmonary hypertension.
Descripción

Pulmonary Hypertension

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0020542
8. patients with known hypersensitivity to any component of definity (r) microbubble contrast.
Descripción

Patients with known hypersensitivity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0020517
9. patients who are pregnant, breast-feeding or are planning to become pregnant during the study duration.
Descripción

Patients who are pregnant

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3242212

Similar models

Eligibility Breast Cancer NCT01817374

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Adult patients
Item
1. adult patients (age 19 years or older).
boolean
C0030705 (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
C0514044 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
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])
Patients who are pregnant
Item
9. patients who are pregnant, breast-feeding or are planning to become pregnant during the study duration.
boolean
C3242212 (UMLS CUI [1])

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