Eligibility Breast Cancer NCT01817374

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Adult patients

Datatype

boolean

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

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

Datatype

boolean

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

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0514044
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

Any history of prior radiation or chemotherapy for breast cancer

Datatype

boolean

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

Patients who only have non-measurable disease

Datatype

boolean

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

Patients who are medically unstable

Datatype

boolean

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

Primary malignant neoplasm

Datatype

boolean

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

Cardiac shunt

Datatype

boolean

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

Patients with unstable cardiopulmonary conditions

Datatype

boolean

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

Pulmonary Hypertension

Datatype

boolean

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

Patients with known hypersensitivity

Datatype

boolean

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

Patients who are pregnant

Datatype

boolean

Alias
UMLS CUI [1]
C3242212

Similar models

Eligibility Breast Cancer NCT01817374

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])