Informationen:
Fehler:
ID
16391
Beschreibung
Radiation Therapy During Surgery in Treating Older Women With Stage I Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00556777
Link
https://clinicaltrials.gov/show/NCT00556777
Stichworte
Versionen (1)
- 14.07.16 14.07.16 -
Hochgeladen am
14. Juli 2016
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00556777
Eligibility Breast Cancer NCT00556777
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Cancer NCT00556777
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Carcinoma breast stage I
Item
histologically confirmed stage i breast cancer
boolean
C0278485 (UMLS CUI [1])
Tumor size | Ultrasonics (sound) | Node stage N0 | Breast quadrant Any
Item
size ≤ 20 mm (by ultrasound), n0, any quadrant
boolean
C0475440 (UMLS CUI [1])
C1456803 (UMLS CUI [2])
C0441959 (UMLS CUI [3])
C0447660 (UMLS CUI [4,1])
C1552551 (UMLS CUI [4,2])
C1456803 (UMLS CUI [2])
C0441959 (UMLS CUI [3])
C0447660 (UMLS CUI [4,1])
C1552551 (UMLS CUI [4,2])
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])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
distant metastases
Item
distant metastases
boolean
C3258247 (UMLS CUI [1])
Inflammatory Breast Carcinoma
Item
inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1])
Lobular carcinoma in situ of breast
Item
lobular in situ disease
boolean
C0279563 (UMLS CUI [1])
invasive cancer | Noninfiltrating Intraductal Carcinoma
Item
invasive cancer or ductal carcinoma in situ
boolean
C0677898 (UMLS CUI [1])
C0007124 (UMLS CUI [2])
C0007124 (UMLS CUI [2])
Breast Carcinoma | Sarcoma
Item
nonepithelial disease or sarcoma
boolean
C0678222 (UMLS CUI [1])
C1261473 (UMLS CUI [2])
C1261473 (UMLS CUI [2])
Multicentric Breast Carcinoma
Item
multicentric disease
boolean
C2986664 (UMLS CUI [1])
Embolism Lymphatic
Item
lymphatic embolism
boolean
C0013922 (UMLS CUI [1,1])
C1522604 (UMLS CUI [1,2])
C1522604 (UMLS CUI [1,2])
margin of safety Unknown | margin of safety Positive | In situ cancer | invasive cancer
Item
margins of safety unknown or positive (in situ or invasive)
boolean
C0243168 (UMLS CUI [1,1])
C0439673 (UMLS CUI [1,2])
C0243168 (UMLS CUI [2,1])
C1446409 (UMLS CUI [2,2])
C0851135 (UMLS CUI [3])
C0677898 (UMLS CUI [4])
C0439673 (UMLS CUI [1,2])
C0243168 (UMLS CUI [2,1])
C1446409 (UMLS CUI [2,2])
C0851135 (UMLS CUI [3])
C0677898 (UMLS CUI [4])
Mammography Preoperative | Breast Microcalcification Diffuse
Item
preoperative mammography showing diffuse microcalcification
boolean
C0024671 (UMLS CUI [1,1])
C0445204 (UMLS CUI [1,2])
C0520594 (UMLS CUI [2,1])
C0205219 (UMLS CUI [2,2])
C0445204 (UMLS CUI [1,2])
C0520594 (UMLS CUI [2,1])
C0205219 (UMLS CUI [2,2])
patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Menopause
Item
menopausal
boolean
C0455962 (UMLS CUI [1])
Karnofsky Performance Status
Item
karnofsky 70-100%
boolean
C0206065 (UMLS CUI [1])
Malignant Neoplasms | Basal cell carcinoma | malignant epithelioma of uterus In situ | Malignant Neoplasm In complete remission
Item
no other prior cancer except basal cell skin cancer, uterine epithelioma in situ, or other cancer in complete remission for the past 5 years
boolean
C0006826 (UMLS CUI [1])
C0007117 (UMLS CUI [2])
C2211949 (UMLS CUI [3,1])
C0444498 (UMLS CUI [3,2])
C0006826 (UMLS CUI [4,1])
C0677874 (UMLS CUI [4,2])
C0007117 (UMLS CUI [2])
C2211949 (UMLS CUI [3,1])
C0444498 (UMLS CUI [3,2])
C0006826 (UMLS CUI [4,1])
C0677874 (UMLS CUI [4,2])
Reasons Study Subject Participation Status Limited
Item
no geographic, social, or psychiatric reasons that would impede participation in study treatment
boolean
C0392360 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
disease characteristic
Item
see disease characteristics
boolean
C0599878 (UMLS CUI [1])
Neoadjuvant Therapy
Item
no prior neoadjuvant therapy
boolean
C0600558 (UMLS CUI [1])
Study Subject Participation Status
Item
no concurrent participation in another study
boolean
C2348568 (UMLS CUI [1])