ID

31433

Descripción

DC Vaccine Therapy Combined With Cytokine-Induced Killer Cell in Treating Patients With Renal Cell Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00862303

Link

https://clinicaltrials.gov/show/NCT00862303

Palabras clave

Versiones (1)
  1. 21/8/18 21/8/18 - Sarah Riepenhausen
Titular de derechos de autor

Fuzhou General Hospital

Subido en

21 de agosto de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0
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Eligibility Renal Cell Carcinoma NCT00862303

Inglés

Eligibility Renal Cell Carcinoma NCT00862303

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically proven renal cell carcinoma
Descripción

Histological determination of a renal cell carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0449575
UMLS CUI [1,2]
C0007134
age: > 18
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
who- ecog performance status 0-1
Descripción

ECOG perfomance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
at least one measurable tumor lesions according to the recist criteria.
Descripción

Measurable tumor lesions according to the recist criteria

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1709926
UMLS CUI [1,2]
C1513041
life expectancy more than 3 months
Descripción

Life expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a history of any other neoplastic disease less than 5 years ago (excepting treated carcinomas in situ of the cervix and basal/squamous cell carcinomas of the skin).
Descripción

History of another neoplastic disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2735087
patients with metastatic disease in the central nervous system (cns).
Descripción

CNS metastasis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0686377
patients with other significant illness including severe allergy, asthma, angina pectoris or congestive heart failure.
Descripción

Concomitant significant illness

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0243087
UMLS CUI [2]
C2945656
UMLS CUI [3]
C0004096
UMLS CUI [4]
C0002962
UMLS CUI [5]
C0018802
patients with acute or chronic infection including hiv.
Descripción

Acute or chronic infection

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3714514
UMLS CUI [2]
C0019682
patients who are pregnant or nursing.
Descripción

Pregnancy or breast feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients who have received antineoplastic therapy including chemotherapy or immunotherapy less than 4 weeks before beginning the trial.
Descripción

Prior antineoplastic therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2346834
patients who receive corticosteroids or other immunosuppressive agents.
Descripción

Corticoid or immunosuppressive therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021079
UMLS CUI [2]
C0239126
patients with active autoimmune diseases such as lupus erythematosus, rheumatoid arthritis or thyroiditis.
Descripción

Concomitant autoimmune diseases

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004364
UMLS CUI [2]
C0409974
UMLS CUI [3]
C0003873
UMLS CUI [4]
C0920350
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Similar models

Eligibility Renal Cell Carcinoma NCT00862303

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Histological determination of a renal cell carcinoma
Item
histologically proven renal cell carcinoma
boolean
C0449575 (UMLS CUI [1,1])
C0007134 (UMLS CUI [1,2])
Age
Item
age: > 18
boolean
C0001779 (UMLS CUI [1])
ECOG perfomance status
Item
who- ecog performance status 0-1
boolean
C1520224 (UMLS CUI [1])
Measurable tumor lesions according to the recist criteria
Item
at least one measurable tumor lesions according to the recist criteria.
boolean
C1709926 (UMLS CUI [1,1])
C1513041 (UMLS CUI [1,2])
Life expectancy
Item
life expectancy more than 3 months
boolean
C0023671 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
History of another neoplastic disease
Item
patients with a history of any other neoplastic disease less than 5 years ago (excepting treated carcinomas in situ of the cervix and basal/squamous cell carcinomas of the skin).
boolean
C2735087 (UMLS CUI [1])
CNS metastasis
Item
patients with metastatic disease in the central nervous system (cns).
boolean
C0686377 (UMLS CUI [1])
Concomitant significant illness
Item
patients with other significant illness including severe allergy, asthma, angina pectoris or congestive heart failure.
boolean
C0243087 (UMLS CUI [1])
C2945656 (UMLS CUI [2])
C0004096 (UMLS CUI [3])
C0002962 (UMLS CUI [4])
C0018802 (UMLS CUI [5])
Acute or chronic infection
Item
patients with acute or chronic infection including hiv.
boolean
C3714514 (UMLS CUI [1])
C0019682 (UMLS CUI [2])
Pregnancy or breast feeding
Item
patients who are pregnant or nursing.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Prior antineoplastic therapy
Item
patients who have received antineoplastic therapy including chemotherapy or immunotherapy less than 4 weeks before beginning the trial.
boolean
C2346834 (UMLS CUI [1])
Corticoid or immunosuppressive therapy
Item
patients who receive corticosteroids or other immunosuppressive agents.
boolean
C0021079 (UMLS CUI [1])
C0239126 (UMLS CUI [2])
Concomitant autoimmune diseases
Item
patients with active autoimmune diseases such as lupus erythematosus, rheumatoid arthritis or thyroiditis.
boolean
C0004364 (UMLS CUI [1])
C0409974 (UMLS CUI [2])
C0003873 (UMLS CUI [3])
C0920350 (UMLS CUI [4])
Volver a la parte superior de la página 

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