ID

36943

Description

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

Lien

https://clinicaltrials.gov/show/NCT02338700

Mots-clés

  1. 22/06/2019 22/06/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

22 juin 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Prostatic Neoplasms NCT02338700

Eligibility Prostatic Neoplasms NCT02338700

Inclusion Criteria
Description

Inclusion Criteria

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

Prostate carcinoma

Type de données

boolean

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

Evaluable Disease Imaging study

Type de données

boolean

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

Immunodeficiency Absent

Type de données

boolean

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

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

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

Informed Consent Unable | Informed Consent Unwilling

Type de données

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
Description

Autoimmune Disease | Prednisone | Immunosuppressive Agents

Type de données

boolean

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

HIV Seropositivity | Positive rpr

Type de données

boolean

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

Pregnancy | Breast Feeding

Type de données

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
Description

Study Subject Participation Status Inappropriate

Type de données

boolean

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

Cancer Vaccine | Biological Immunotherapy

Type de données

boolean

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

Hypersensitivity Ingredient Vaccine Mixed

Type de données

boolean

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

Similar models

Eligibility Prostatic Neoplasms NCT02338700

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])

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