ID

44644

Descripción

Radiation Therapy in Treating Women With Invasive Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00301041

Link

https://clinicaltrials.gov/show/NCT00301041

Palabras clave

Versiones (2)
  1. 12/7/16 12/7/16 -
  2. 27/9/21 27/9/21 -
Subido en

27 de septiembre de 2021

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00301041

Inglés

Eligibility Breast Cancer NCT00301041

1 formularios  
Criteria
Descripción

Criteria

histologically confirmed invasive breast cancer
Descripción

Invasive carcinoma of breast

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0853879
underwent lumpectomy (breast-preserving surgery) with or without adjuvant chemotherapy within the past 12 weeks
Descripción

Lumpectomy | Breast-Conserving Surgery | Chemotherapy, Adjuvant

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0740370
UMLS CUI [2]
C0917927
UMLS CUI [3]
C0085533
histologically negative surgical margins (i.e., no tumor on ink)
Descripción

Surgical margins Negative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0229985
UMLS CUI [1,2]
C0205160
candidates for postoperative breast radiotherapy
Descripción

Indication Radiotherapy to breast Postoperative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0948310
UMLS CUI [1,3]
C0032790
determined not to need radiotherapy to regional nodes (e.g., third supraclavicular field)
Descripción

Therapeutic radiology procedure Regional lymph nodes Patient need for

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C1179441
UMLS CUI [1,3]
C0686904
hormone receptor status not specified
Descripción

Hormone Receptor Status Unspecified

Tipo de datos

boolean

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

Patient Characteristics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0815172
female
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
menopausal status not specified
Descripción

Menopausal Status Unspecified

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3829127
UMLS CUI [1,2]
C0205370
not pregnant or nursing
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
negative pregnancy test
Descripción

Pregnancy test negative

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0427780
fertile patients must use effective contraception
Descripción

Fertility Contraceptive methods

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0015895
UMLS CUI [1,2]
C0700589
no history of scleroderma or systemic lupus erythematosis
Descripción

Scleroderma | Lupus Erythematosus, Systemic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011644
UMLS CUI [2]
C0024141
no other prior or concurrent malignancy except nonmelanoma skin cancer or carcinoma in situ of the cervix
Descripción

Malignant Neoplasms | Skin carcinoma | Carcinoma in situ of uterine cervix

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0699893
UMLS CUI [3]
C0851140
prior concurrent therapy:
Descripción

concurrent therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009429
see disease characteristics
Descripción

disease characteristic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0599878
no prior breast radiotherapy
Descripción

Radiotherapy to breast

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0948310
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Similar models

Eligibility Breast Cancer NCT00301041

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Invasive carcinoma of breast
Item
histologically confirmed invasive breast cancer
boolean
C0853879 (UMLS CUI [1])
Lumpectomy | Breast-Conserving Surgery | Chemotherapy, Adjuvant
Item
underwent lumpectomy (breast-preserving surgery) with or without adjuvant chemotherapy within the past 12 weeks
boolean
C0740370 (UMLS CUI [1])
C0917927 (UMLS CUI [2])
C0085533 (UMLS CUI [3])
Surgical margins Negative
Item
histologically negative surgical margins (i.e., no tumor on ink)
boolean
C0229985 (UMLS CUI [1,1])
C0205160 (UMLS CUI [1,2])
Indication Radiotherapy to breast Postoperative
Item
candidates for postoperative breast radiotherapy
boolean
C3146298 (UMLS CUI [1,1])
C0948310 (UMLS CUI [1,2])
C0032790 (UMLS CUI [1,3])
Therapeutic radiology procedure Regional lymph nodes Patient need for
Item
determined not to need radiotherapy to regional nodes (e.g., third supraclavicular field)
boolean
C1522449 (UMLS CUI [1,1])
C1179441 (UMLS CUI [1,2])
C0686904 (UMLS CUI [1,3])
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])
Patient Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C3829127 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Pregnancy test negative
Item
negative pregnancy test
boolean
C0427780 (UMLS CUI [1])
Fertility Contraceptive methods
Item
fertile patients must use effective contraception
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Scleroderma | Lupus Erythematosus, Systemic
Item
no history of scleroderma or systemic lupus erythematosis
boolean
C0011644 (UMLS CUI [1])
C0024141 (UMLS CUI [2])
Malignant Neoplasms | Skin carcinoma | Carcinoma in situ of uterine cervix
Item
no other prior or concurrent malignancy except nonmelanoma skin cancer or carcinoma in situ of the cervix
boolean
C0006826 (UMLS CUI [1])
C0699893 (UMLS CUI [2])
C0851140 (UMLS CUI [3])
concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
disease characteristic
Item
see disease characteristics
boolean
C0599878 (UMLS CUI [1])
Radiotherapy to breast
Item
no prior breast radiotherapy
boolean
C0948310 (UMLS CUI [1])
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