Information:
Error:
ID
44644
Description
Radiation Therapy in Treating Women With Invasive Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00301041
Link
https://clinicaltrials.gov/show/NCT00301041
Keywords
Versions (2)
- 7/12/16 7/12/16 -
- 9/27/21 9/27/21 -
Uploaded on
September 27, 2021
DOI
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License
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00301041
Eligibility Breast Cancer NCT00301041
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00301041
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
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])
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])
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])
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])
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])
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])
C0205370 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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])
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])
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])
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])