Informações:
Falhas:
ID
23576
Descrição
Breast-Conserving Surgery Techniques in Treating Women With Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00870415
Link
https://clinicaltrials.gov/show/NCT00870415
Palavras-chave
Versões (1)
- 09/07/2017 09/07/2017 -
Transferido a
9 de julho de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00870415
Eligibility Breast Cancer NCT00870415
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00870415
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Criteria Fulfill
Item
meets 1 of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
C0679823 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])