Eligibility Breast Cancer NCT00093002

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
postmenopausal women defined as women who have stopped having menstrual periods
Descripción

postmenopausal women

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232970
written informed consent to participate in the trial
Descripción

written informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
biopsy confirmation of invasive breast cancer
Descripción

Biopsy result

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0405352
UMLS CUI [1,2]
C0853879
evidence of hormone sensitivity
Descripción

Hormone status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0920555
willingness to undergo biopsies
Descripción

willingness to undergo biopsies

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0405352
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
any previous treatment for breast cancer
Descripción

previous treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1511300
unwillingness to stop taking any drug known to affect sex hormonal status or a patient in which it would be inappropriate to stop.
Descripción

ID.7

Tipo de datos

boolean

any severe concurrent condition that would preclude surgery or that would jeopardize compliance with the study, e.g., uncontrolled cardiac disease or uncontrolled diabetes mellitus
Descripción

Comorbidities

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009488
the presence of more than one primary tumor
Descripción

Number of primary tumors

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0449788
UMLS CUI [1,2]
C0677930
history of hypersensitivity to castor oil
Descripción

hypersensitivity to castor oil

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0007343
history of known bleeding disorders
Descripción

bleeding disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005779

Similar models

Eligibility Breast Cancer NCT00093002

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
postmenopausal women
Item
postmenopausal women defined as women who have stopped having menstrual periods
boolean
C0232970 (UMLS CUI [1])
written informed consent
Item
written informed consent to participate in the trial
boolean
C0021430 (UMLS CUI [1])
Biopsy result
Item
biopsy confirmation of invasive breast cancer
boolean
C0405352 (UMLS CUI [1,1])
C0853879 (UMLS CUI [1,2])
Hormone status
Item
evidence of hormone sensitivity
boolean
C0920555 (UMLS CUI [1])
willingness to undergo biopsies
Item
willingness to undergo biopsies
boolean
C0021430 (UMLS CUI [1,1])
C0405352 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
previous treatment
Item
any previous treatment for breast cancer
boolean
C1511300 (UMLS CUI [1])
ID.7
Item
unwillingness to stop taking any drug known to affect sex hormonal status or a patient in which it would be inappropriate to stop.
boolean
Comorbidities
Item
any severe concurrent condition that would preclude surgery or that would jeopardize compliance with the study, e.g., uncontrolled cardiac disease or uncontrolled diabetes mellitus
boolean
C0009488 (UMLS CUI [1])
Number of primary tumors
Item
the presence of more than one primary tumor
boolean
C0449788 (UMLS CUI [1,1])
C0677930 (UMLS CUI [1,2])
hypersensitivity to castor oil
Item
history of hypersensitivity to castor oil
boolean
C0020517 (UMLS CUI [1,1])
C0007343 (UMLS CUI [1,2])
bleeding disorders
Item
history of known bleeding disorders
boolean
C0005779 (UMLS CUI [1])