ID

20439

Description

Tamoxifen Resistance in Women With Stage I, Stage II, Stage IIIA, or Stage IIIB Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00899197

Link

https://clinicaltrials.gov/show/NCT00899197

Keywords

  1. 2/22/17 2/22/17 -
Uploaded on

February 22, 2017

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00899197

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])

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