Eligibility Breast Cancer NCT00899197

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed invasive breast cancer
Description

histologically confirmed invasive breast cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C0853879
UMLS CUI [1,2]
C0679557
initial pathologic stage i-iiib disease
Description

tumor stage

Data type

boolean

Alias
UMLS CUI [1]
C1300072
no stage iv disease
Description

tumor stage

Data type

boolean

Alias
UMLS CUI [1]
C1300072
meets the following criteria for breast cancer therapy:
Description

ID.4

Data type

boolean

received prior primary local therapy for breast cancer
Description

received prior primary local therapy for breast cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C1517925
UMLS CUI [1,3]
C0678222
scheduled to begin tamoxifen citrate as adjuvant therapy for breast cancer within 3 weeks
Description

tamoxifen, adjuvant therapy, breast cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C0039286
UMLS CUI [1,2]
C0677850
UMLS CUI [1,3]
C0678222
hormone receptor status:
Description

hormone receptor status

Data type

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
estrogen-receptor positive tumor
Description

estrogen receptor status

Data type

boolean

Alias
UMLS CUI [1]
C1719706
female
Description

gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
pre- or post-menopausal
Description

menopausal status

Data type

boolean

Alias
UMLS CUI [1]
C0455962
must be able to donate 20 ml of blood
Description

able to donate blood

Data type

boolean

Alias
UMLS CUI [1]
C0425264
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe anemia, defined as hemoglobin < 11 g/dl
Description

hemoglobin, severe anemia

Data type

boolean

Alias
UMLS CUI [1,1]
C0019046
UMLS CUI [1,2]
C0238644
psychiatric history that would preclude obtaining informed consent
Description

psychiatric history, informed consent

Data type

boolean

Alias
UMLS CUI [1,1]
C0748059
UMLS CUI [1,2]
C0021430

Similar models

Eligibility Breast Cancer NCT00899197

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
histologically confirmed invasive breast cancer
Item
histologically confirmed invasive breast cancer
boolean
C0853879 (UMLS CUI [1,1])
C0679557 (UMLS CUI [1,2])
tumor stage
Item
initial pathologic stage i-iiib disease
boolean
C1300072 (UMLS CUI [1])
tumor stage
Item
no stage iv disease
boolean
C1300072 (UMLS CUI [1])
ID.4
Item
meets the following criteria for breast cancer therapy:
boolean
received prior primary local therapy for breast cancer
Item
received prior primary local therapy for breast cancer
boolean
C1514463 (UMLS CUI [1,1])
C1517925 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
tamoxifen, adjuvant therapy, breast cancer
Item
scheduled to begin tamoxifen citrate as adjuvant therapy for breast cancer within 3 weeks
boolean
C0039286 (UMLS CUI [1,1])
C0677850 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
hormone receptor status
Item
hormone receptor status:
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
estrogen receptor status
Item
estrogen-receptor positive tumor
boolean
C1719706 (UMLS CUI [1])
gender
Item
female
boolean
C0079399 (UMLS CUI [1])
menopausal status
Item
pre- or post-menopausal
boolean
C0455962 (UMLS CUI [1])
able to donate blood
Item
must be able to donate 20 ml of blood
boolean
C0425264 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
hemoglobin, severe anemia
Item
severe anemia, defined as hemoglobin < 11 g/dl
boolean
C0019046 (UMLS CUI [1,1])
C0238644 (UMLS CUI [1,2])
psychiatric history, informed consent
Item
psychiatric history that would preclude obtaining informed consent
boolean
C0748059 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])