ID

36943

Descripción

Safety and Efficacy Study of Mix Vaccine in Prostate Carcinoma Patient; ODM derived from: https://clinicaltrials.gov/show/NCT02338700

Link

https://clinicaltrials.gov/show/NCT02338700

Palabras clave

Versiones (1)
  1. 22/6/19 22/6/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

22 de junio de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Prostatic Neoplasms NCT02338700

Inglés

Eligibility Prostatic Neoplasms NCT02338700

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients diagnosed with prostate carcinoma based on histology
Descripción

Prostate carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0600139
evaluable lesions on imaging study
Descripción

Evaluable Disease Imaging study

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1516986
UMLS CUI [1,2]
C1881134
without known immunodeficiency
Descripción

Immunodeficiency Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021051
UMLS CUI [1,2]
C0332197
age >18 and <80 years ago
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients is unable or unwilling to sign informed consent
Descripción

Informed Consent Unable | Informed Consent Unwilling

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080
any autoimmune disorder, which is currently being treated with prednisone or any other immune suppressive medication
Descripción

Autoimmune Disease | Prednisone | Immunosuppressive Agents

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004364
UMLS CUI [2]
C0032952
UMLS CUI [3]
C0021081
positive hiv and/or rpr (rapid plasma reagin)
Descripción

HIV Seropositivity | Positive rpr

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019699
UMLS CUI [2]
C0240917
female patient who is pregnant or breast feeding
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients, based on the opinion pf the investigator, should not be enrolled into this study
Descripción

Study Subject Participation Status Inappropriate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788
prior anti-cancer vaccine or biological immunotherapy
Descripción

Cancer Vaccine | Biological Immunotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0376659
UMLS CUI [2]
C1511146
allergic to any known ingredient of the mv compound
Descripción

Hypersensitivity Ingredient Vaccine Mixed

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1550600
UMLS CUI [1,3]
C0042210
UMLS CUI [1,4]
C0205430
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Similar models

Eligibility Prostatic Neoplasms NCT02338700

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Prostate carcinoma
Item
patients diagnosed with prostate carcinoma based on histology
boolean
C0600139 (UMLS CUI [1])
Evaluable Disease Imaging study
Item
evaluable lesions on imaging study
boolean
C1516986 (UMLS CUI [1,1])
C1881134 (UMLS CUI [1,2])
Immunodeficiency Absent
Item
without known immunodeficiency
boolean
C0021051 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Age
Item
age >18 and <80 years ago
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Informed Consent Unable | Informed Consent Unwilling
Item
patients is unable or unwilling to sign informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Autoimmune Disease | Prednisone | Immunosuppressive Agents
Item
any autoimmune disorder, which is currently being treated with prednisone or any other immune suppressive medication
boolean
C0004364 (UMLS CUI [1])
C0032952 (UMLS CUI [2])
C0021081 (UMLS CUI [3])
HIV Seropositivity | Positive rpr
Item
positive hiv and/or rpr (rapid plasma reagin)
boolean
C0019699 (UMLS CUI [1])
C0240917 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
female patient who is pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status Inappropriate
Item
patients, based on the opinion pf the investigator, should not be enrolled into this study
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
Cancer Vaccine | Biological Immunotherapy
Item
prior anti-cancer vaccine or biological immunotherapy
boolean
C0376659 (UMLS CUI [1])
C1511146 (UMLS CUI [2])
Hypersensitivity Ingredient Vaccine Mixed
Item
allergic to any known ingredient of the mv compound
boolean
C0020517 (UMLS CUI [1,1])
C1550600 (UMLS CUI [1,2])
C0042210 (UMLS CUI [1,3])
C0205430 (UMLS CUI [1,4])
Volver a la parte superior de la página 

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