ID

14882

Descripción

Safety and Efficacy Study of Mix Vaccine in Breast Carcinoma Patient; ODM derived from: https://clinicaltrials.gov/show/NCT02338804

Link

https://clinicaltrials.gov/show/NCT02338804

Palabras clave

Versiones (1)
  1. 3/5/16 3/5/16 -
Subido en

3 de mayo de 2016

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT02338804

Inglés

Eligibility Breast Neoplasms NCT02338804

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
1.patients diagnosed with breast carcinoma based on histology
Descripción

Breast Carcinoma Histologic

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205462
2.evaluable lesions on imaging study
Descripción

Evaluable Disease Lesion | imaging studies

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1516986
UMLS CUI [1,2]
C0221198
UMLS CUI [2]
C1881134
3.without known immunodeficiency
Descripción

Immunologic Deficiency Syndromes

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021051
4.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
1.patients is unable or unwilling to sign informed consent
Descripción

Unable Informed Consent

Tipo de datos

boolean

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

Autoimmune Diseases Prednisone treatment | Immunosuppressive drug

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004364
UMLS CUI [1,2]
C0747791
UMLS CUI [2]
C0499076
3.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
4.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
5.patients, based on the opinion pf the investigator, should not be enrolled into this study
Descripción

patient not eligible | clinical research investigator

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3242266
UMLS CUI [2]
C1552025
6.prior anti-cancer vaccine or biological immunotherapy
Descripción

Vaccines Cancer treatment | Biological Immunotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0042210
UMLS CUI [1,2]
C0920425
UMLS CUI [2]
C1511146
7.allergic to any known ingredient of the mv compound
Descripción

Hypersensitivity Chemical Ingredients Investigational New Drug

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0085993
UMLS CUI [1,3]
C0013230
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Similar models

Eligibility Breast Neoplasms NCT02338804

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Breast Carcinoma Histologic
Item
1.patients diagnosed with breast carcinoma based on histology
boolean
C0678222 (UMLS CUI [1,1])
C0205462 (UMLS CUI [1,2])
Evaluable Disease Lesion | imaging studies
Item
2.evaluable lesions on imaging study
boolean
C1516986 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C1881134 (UMLS CUI [2])
Immunologic Deficiency Syndromes
Item
3.without known immunodeficiency
boolean
C0021051 (UMLS CUI [1])
Age
Item
4.age >18 and <80 years ago
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Unable Informed Consent
Item
1.patients is unable or unwilling to sign informed consent
boolean
C1299582 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Autoimmune Diseases Prednisone treatment | Immunosuppressive drug
Item
2.any autoimmune disorder, which is currently being treated with prednisone or any other immune suppressive medication
boolean
C0004364 (UMLS CUI [1,1])
C0747791 (UMLS CUI [1,2])
C0499076 (UMLS CUI [2])
HIV Seropositivity | Positive rpr
Item
3.positive hiv and/or rpr (rapid plasma reagin)
boolean
C0019699 (UMLS CUI [1])
C0240917 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
4.female patient who is pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
patient not eligible | clinical research investigator
Item
5.patients, based on the opinion pf the investigator, should not be enrolled into this study
boolean
C3242266 (UMLS CUI [1])
C1552025 (UMLS CUI [2])
Vaccines Cancer treatment | Biological Immunotherapy
Item
6.prior anti-cancer vaccine or biological immunotherapy
boolean
C0042210 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C1511146 (UMLS CUI [2])
Hypersensitivity Chemical Ingredients Investigational New Drug
Item
7.allergic to any known ingredient of the mv compound
boolean
C0020517 (UMLS CUI [1,1])
C0085993 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,3])
Volver a la parte superior de la página 

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