Informazione:
Errore:
ID
19702
Descrizione
Enzastaurin For Breast Cancer Patients Who Previously Received an Anthracycline and a Taxane Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT00386087
collegamento
https://clinicaltrials.gov/show/NCT00386087
Keywords
versioni (1)
- 23/01/17 23/01/17 -
Caricato su
23 gennaio 2017
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT00386087
Eligibility Breast Neoplasms NCT00386087
- StudyEvent: Eligibility
Similar models
Eligibility Breast Neoplasms NCT00386087
- StudyEvent: Eligibility
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Secondary malignant neoplasm of female breast Inoperable Curative | Breast cancer recurrent Inoperable Curative
Item
clinical diagnosis of metastatic breast cancer or recurrent breast cancer where surgery can not be done for curative intent
boolean
C0346993 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C1276305 (UMLS CUI [1,3])
C0278493 (UMLS CUI [2,1])
C0205187 (UMLS CUI [2,2])
C1276305 (UMLS CUI [2,3])
C0205187 (UMLS CUI [1,2])
C1276305 (UMLS CUI [1,3])
C0278493 (UMLS CUI [2,1])
C0205187 (UMLS CUI [2,2])
C1276305 (UMLS CUI [2,3])
Anthracyclines Class of Trial Agent | taxane Class of Trial Agent
Item
have received prior therapy with an anthracycline (class of drugs) and a taxane (class of drugs).
boolean
C0282564 (UMLS CUI [1,1])
C2983595 (UMLS CUI [1,2])
C0215136 (UMLS CUI [2,1])
C2983595 (UMLS CUI [2,2])
C2983595 (UMLS CUI [1,2])
C0215136 (UMLS CUI [2,1])
C2983595 (UMLS CUI [2,2])
HER2-positive carcinoma of breast Herceptin Excluded
Item
tumors must not be positive for her2, but if positive, the treatment plan should not include further treatment with the drug herceptin.
boolean
C1960398 (UMLS CUI [1,1])
C0338204 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
C0338204 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
Measurable Disease X-Ray Computed Tomography | Radiology test
Item
disease that can be definitely measured on cat scans or other radiological tests.
boolean
C1513041 (UMLS CUI [1,1])
C0040405 (UMLS CUI [1,2])
C0807679 (UMLS CUI [2])
C0040405 (UMLS CUI [1,2])
C0807679 (UMLS CUI [2])
High-Dose Chemotherapy with Autologous Stem Cell Transplant
Item
may have received high dose chemotherapy for autologous stem cell support greater than or equal to 6 months of starting this study.
boolean
C1512429 (UMLS CUI [1])
Chemotherapy Regimen Quantity Neoplasm Metastasis | Chemotherapy Regimen Quantity Recurrent disease Local
Item
more than 2 chemotherapy regimens for metastatic or locally recurrent disease.
boolean
C0392920 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0027627 (UMLS CUI [1,3])
C0392920 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0277556 (UMLS CUI [2,3])
C0205276 (UMLS CUI [2,4])
C1265611 (UMLS CUI [1,2])
C0027627 (UMLS CUI [1,3])
C0392920 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0277556 (UMLS CUI [2,3])
C0205276 (UMLS CUI [2,4])
Malignant neoplasm of brain Due to Breast Carcinoma
Item
have brain cancer from breast cancer
boolean
C0153633 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
C0678226 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Able to swallow Tablets
Item
have an inability to swallow tablets
boolean
C2712086 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
Heart condition Serious
Item
within 6 months have had a serious heart condition
boolean
C3842523 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0205404 (UMLS CUI [1,2])