Información:
Error:
ID
12921
Descripción
Gene Therapy Plus Chemotherapy in Treating Patients With Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00004038
Link
https://clinicaltrials.gov/show/NCT00004038
Palabras clave
Versiones (1)
- 6/1/16 6/1/16 -
Titular de derechos de autor
CC BY-NC 3.0
Subido en
6 de enero de 2016
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 3.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
Eligibility Breast Cancer NCT00004038
Eligibility Breast Cancer NCT00004038
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00004038
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
breast cancer
Item
histologically confirmed epithelial breast cancer
boolean
C0678222 (UMLS CUI [1])
cutaneous or subcutaneous lesions
Item
at least 3 cutaneous or subcutaneous lesions required
boolean
C0221198 (UMLS CUI [1])
measurable disease
Item
measurable disease that includes, but is not limited to, cutaneous or subcutaneous metastases
boolean
C1513041 (UMLS CUI [1])
patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
age
Item
age: over 18
boolean
C0001779 (UMLS CUI [1])
performance status
Item
performance status: ecog 0-2
boolean
C1520224 (UMLS CUI [1])
absolute granulocyte count
Item
absolute granulocyte count at least 1,500/mm3
boolean
C0857490 (UMLS CUI [1])
hemoglobin
Item
hemoglobin greater than 8 g/dl
boolean
C0019046 (UMLS CUI [1])
platelet count
Item
platelet count greater than 100,000/mm3
boolean
C0005821 (UMLS CUI [1])
bilirubin
Item
bilirubin less than 2 mg/dl
boolean
C1278039 (UMLS CUI [1])
pt/ptt
Item
pt/ptt within normal range
boolean
C0030605 (UMLS CUI [1])
sgot/sgpt
Item
sgot/sgpt less than 2 times upper limit of normal
boolean
C0201836 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201899 (UMLS CUI [2])
creatinine
Item
creatinine less than 1.8 mg/dl
boolean
C0201976 (UMLS CUI [1])
pregnant
Item
not pregnant
boolean
C0032961 (UMLS CUI [1])
contraception
Item
fertile patients must use effective contraception during and for 3 months after therapy
boolean
C0700589 (UMLS CUI [1])
prior concurrent therapy:
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
chemotherapy
Item
concurrent cytotoxic chemotherapy allowed, if stable and responding
boolean
C0392920 (UMLS CUI [1])
at least 4 weeks since prior chemotherapy, if starting a new regimen
Item
at least 4 weeks since prior chemotherapy, if starting a new regimen
boolean
C0392920 (UMLS CUI [1])
radiotherapy
Item
at least 4 weeks since radiotherapy
boolean
C1522449 (UMLS CUI [1])
prior adjuvant radiotherapy to the chest wall allowed
Item
prior adjuvant radiotherapy to the chest wall allowed
boolean
C1522449 (UMLS CUI [1])
at least 6 months since radiotherapy to lesions that are to be injected
Item
at least 6 months since radiotherapy to lesions that are to be injected
boolean
C1522449 (UMLS CUI [1])
recovered from prior therapy
Item
recovered from prior therapy
boolean
C0087111 (UMLS CUI [1])