Eligibility Breast Cancer NCT00870415

Criteria
Description

Criteria

meets 1 of the following criteria:
Description

Criteria Fulfill

Data type

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
diagnosis of intraductal breast cancer requiring a wide local resection
Description

Noninfiltrating Intraductal Carcinoma | Local excision Wide Patient need for

Data type

boolean

Alias
UMLS CUI [1]
C0007124
UMLS CUI [2,1]
C0278259
UMLS CUI [2,2]
C0332464
UMLS CUI [2,3]
C0686904
diagnosis of infiltrating ductal breast cancer within range
Description

Invasive Ductal Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C1134719
diagnosis of invasive breast cancer that has not responded well to neoadjuvant treatment
Description

Invasive carcinoma of breast | Neoadjuvant Therapy Poor response

Data type

boolean

Alias
UMLS CUI [1]
C0853879
UMLS CUI [2,1]
C0600558
UMLS CUI [2,2]
C1320680
no multicentric tumor
Description

Malignant Neoplasm Multicentric Exclusion

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0439743
UMLS CUI [1,3]
C2828389
no gigantomastia
Description

Gigantomastia Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0392533
UMLS CUI [1,2]
C2828389
hormone receptor status not specified
Description

Hormone Receptor Status Unspecified

Data type

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0205370
patient characteristics:
Description

Client Characteristics

Data type

boolean

Alias
UMLS CUI [1]
C0815172
menopausal status not specified
Description

Menopausal state Unspecified

Data type

boolean

Alias
UMLS CUI [1,1]
C0025320
UMLS CUI [1,2]
C0205370
no patients subject to a measure of legal protection or unable to express consent
Description

Involvement with Legal intervention Excluded | Informed Consent Unable Exclusion

Data type

boolean

Alias
UMLS CUI [1,1]
C1314939
UMLS CUI [1,2]
C0178362
UMLS CUI [1,3]
C2828389
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
UMLS CUI [2,3]
C2828389
no patients deprived of liberty by judicial or administrative decision or hospitalized without patient consent
Description

Deprivation Freedom Judicial aspects Exclusion | Hospitalization involuntary Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0871712
UMLS CUI [1,2]
C0016694
UMLS CUI [1,3]
C0243116
UMLS CUI [1,4]
C2828389
UMLS CUI [2,1]
C0745037
UMLS CUI [2,2]
C2828389
not pregnant or nursing
Description

Pregnancy Excluded | Breast Feeding Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C2828389
UMLS CUI [2,1]
C0006147
UMLS CUI [2,2]
C2828389
prior concurrent therapy:
Description

Prior Therapy

Data type

boolean

Alias
UMLS CUI [1]
C1514463
no prior radiotherapy to the diseased breast
Description

Breast Involved Therapeutic radiology procedure Exclusion

Data type

boolean

Alias
UMLS CUI [1,1]
C0006141
UMLS CUI [1,2]
C1314939
UMLS CUI [1,3]
C1522449
UMLS CUI [1,4]
C2828389
no prior adjuvant treatment
Description

Adjuvant therapy Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0677850
UMLS CUI [1,2]
C2828389
no concurrent participation in another clinical research study
Description

Exclusion Participation Clinical Trial other

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C0008976
UMLS CUI [1,4]
C0205394

Similar models

Eligibility Breast Cancer NCT00870415

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Criteria Fulfill
Item
meets 1 of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Noninfiltrating Intraductal Carcinoma | Local excision Wide Patient need for
Item
diagnosis of intraductal breast cancer requiring a wide local resection
boolean
C0007124 (UMLS CUI [1])
C0278259 (UMLS CUI [2,1])
C0332464 (UMLS CUI [2,2])
C0686904 (UMLS CUI [2,3])
Invasive Ductal Breast Carcinoma
Item
diagnosis of infiltrating ductal breast cancer within range
boolean
C1134719 (UMLS CUI [1])
Invasive carcinoma of breast | Neoadjuvant Therapy Poor response
Item
diagnosis of invasive breast cancer that has not responded well to neoadjuvant treatment
boolean
C0853879 (UMLS CUI [1])
C0600558 (UMLS CUI [2,1])
C1320680 (UMLS CUI [2,2])
Malignant Neoplasm Multicentric Exclusion
Item
no multicentric tumor
boolean
C0006826 (UMLS CUI [1,1])
C0439743 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
Gigantomastia Excluded
Item
no gigantomastia
boolean
C0392533 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Menopausal state Unspecified
Item
menopausal status not specified
boolean
C0025320 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
Involvement with Legal intervention Excluded | Informed Consent Unable Exclusion
Item
no patients subject to a measure of legal protection or unable to express consent
boolean
C1314939 (UMLS CUI [1,1])
C0178362 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
C2828389 (UMLS CUI [2,3])
Deprivation Freedom Judicial aspects Exclusion | Hospitalization involuntary Excluded
Item
no patients deprived of liberty by judicial or administrative decision or hospitalized without patient consent
boolean
C0871712 (UMLS CUI [1,1])
C0016694 (UMLS CUI [1,2])
C0243116 (UMLS CUI [1,3])
C2828389 (UMLS CUI [1,4])
C0745037 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
Pregnancy Excluded | Breast Feeding Excluded
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
Prior Therapy
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1])
Breast Involved Therapeutic radiology procedure Exclusion
Item
no prior radiotherapy to the diseased breast
boolean
C0006141 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,3])
C2828389 (UMLS CUI [1,4])
Adjuvant therapy Excluded
Item
no prior adjuvant treatment
boolean
C0677850 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
Exclusion Participation Clinical Trial other
Item
no concurrent participation in another clinical research study
boolean
C2828389 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])