Informações:
Falhas:
ID
26085
Descrição
Intensity Modulated Radiotherapy for Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00594477
Link
https://clinicaltrials.gov/show/NCT00594477
Palavras-chave
Versões (1)
- 09/10/2017 09/10/2017 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
9 de outubro de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00594477
Eligibility Breast Cancer NCT00594477
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00594477
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Gender
Item
female gender
boolean
C0079399 (UMLS CUI [1])
Age
Item
age ≥ 18 years
boolean
C0001779 (UMLS CUI [1])
Invasive carcinoma of breast Primary
Item
invasive primary female breast cancer
boolean
C0853879 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,2])
Secondary malignant neoplasm of lymph node regional
Item
pathologically proven regional nodal metastasis
boolean
C0686619 (UMLS CUI [1,1])
C0205147 (UMLS CUI [1,2])
C0205147 (UMLS CUI [1,2])
Mastectomy Status post | Segmental Mastectomy Status post | Axillary lymph nodes Assessment Sentinel Lymph Node Biopsy | Excision of axillary lymph nodes
Item
status post mastectomy or partial mastectomy with an assessment of axillary nodes via sentinel lymph node biopsy and/or axillary lymph node dissection.
boolean
C0024881 (UMLS CUI [1,1])
C0231290 (UMLS CUI [1,2])
C0024885 (UMLS CUI [2,1])
C0231290 (UMLS CUI [2,2])
C0729594 (UMLS CUI [3,1])
C1516048 (UMLS CUI [3,2])
C0796693 (UMLS CUI [3,3])
C0193867 (UMLS CUI [4])
C0231290 (UMLS CUI [1,2])
C0024885 (UMLS CUI [2,1])
C0231290 (UMLS CUI [2,2])
C0729594 (UMLS CUI [3,1])
C1516048 (UMLS CUI [3,2])
C0796693 (UMLS CUI [3,3])
C0193867 (UMLS CUI [4])
Informed Consent
Item
signed study specific consent form
boolean
C0021430 (UMLS CUI [1])
Distant metastasis
Item
distant metastasis
boolean
C1275402 (UMLS CUI [1])
Pregnancy
Item
currently pregnant
boolean
C0032961 (UMLS CUI [1])
Mental disorders Exclude Informed Consent | Addictive Behavior Excludes Informed Consent
Item
psychiatric or addictive disorders that preclude informed consent
boolean
C0004936 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
C0085281 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,3])
C0332196 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
C0085281 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,3])
Time Interval Initial diagnosis Start Therapeutic radiology procedure
Item
time from initial diagnosis to the start of radiation therapy > one year
boolean
C0872291 (UMLS CUI [1,1])
C4071762 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])
C1522449 (UMLS CUI [1,4])
C4071762 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])
C1522449 (UMLS CUI [1,4])
Life Expectancy
Item
estimated life expectancy judged to be < one year
boolean
C0023671 (UMLS CUI [1])
Prior radiation therapy Breast Ipsilateral | Radiotherapy to chest wall
Item
prior radiation to the ipsilateral breast or chest wall
boolean
C0279134 (UMLS CUI [1,1])
C0006141 (UMLS CUI [1,2])
C0441989 (UMLS CUI [1,3])
C1998066 (UMLS CUI [2])
C0006141 (UMLS CUI [1,2])
C0441989 (UMLS CUI [1,3])
C1998066 (UMLS CUI [2])
Breast Carcinoma Primary | Lymphoma | Sarcoma
Item
primary breast cancer is lymphoma or sarcoma
boolean
C0678222 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0024299 (UMLS CUI [2])
C1261473 (UMLS CUI [3])
C0205225 (UMLS CUI [1,2])
C0024299 (UMLS CUI [2])
C1261473 (UMLS CUI [3])
Chemotherapy Concurrent
Item
patients being treated with concurrent chemotherapy.
boolean
C0392920 (UMLS CUI [1,1])
C0205420 (UMLS CUI [1,2])
C0205420 (UMLS CUI [1,2])