ID

13597

Descrizione

Safety, Immunogenicity and Reactogenicity of Recombinant Hepatitis B Vaccine (Adjuvanted & New Formulation) and Engerix™-B; ODM derived from: https://clinicaltrials.gov/show/NCT00697840

collegamento

https://clinicaltrials.gov/show/NCT00697840

Keywords

  1. 18/02/16 18/02/16 -
Caricato su

18 febbraio 2016

DOI

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Licenza

Creative Commons BY 4.0

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Eligibility Hepatitis B NCT00697840

Eligibility Hepatitis B NCT00697840

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
between 18 and 40 years old.
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
written informed consent will have been obtained from the subjects.
Descrizione

written informed consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
good physical condition as established by physical examination and history taking at the time of entry.
Descrizione

good physical condition

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1142435
female participants will avoid becoming pregnant during the study period and they will have been on a contraceptive program for at least 2 months before entry
Descrizione

pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy or lactation.
Descrizione

pregnancy or lactation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
positive titres for anti hbs antibody.
Descrizione

Hepatitis B surface antibody

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0149708
any vaccination against hepatitis b in the past.
Descrizione

Hepatitis B vaccination

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0474232
any previous administration of mpl.
Descrizione

mpl administration

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0066776
elevated serum liver enzymes.
Descrizione

elevated serum liver enzymes

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1287351
history of significant and persisting hematologic, hepatic, renal, cardiac or respiratory disease.
Descrizione

hematologic, hepatic, renal, cardiac or respiratory disease

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0009488
axillary temperature > 37.5°c at the time of injection.
Descrizione

axillary temperature

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1531924
any acute disease at the moment of entry.
Descrizione

any acute disease

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0009488
chronic alcohol consumption.
Descrizione

chronic alcohol consumption

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0038586
any treatment with immunosuppressive or immunostimulant therapy.
Descrizione

immunosuppressive or immunostimulant

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021079
UMLS CUI [2]
C0001551
any chronic drug treatment, which in the investigator's opinion, precludes inclusion into the study.
Descrizione

drug treatment precluding inclustion into study

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0013216
UMLS CUI [2]
C1321605
history of allergic disease likely to be stimulated by any component of the vaccine.
Descrizione

hypersensitivitiy to vaccine

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1521826
simultaneous administration of any other vaccine(s).
Descrizione

simultaneous administration of any other vaccines

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1321605
administration of any immunoglobulin during the study period.
Descrizione

administration of any immunoglobulin

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1321605
simultaneous participation in any other clinical trial.
Descrizione

study participation status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Hepatitis B NCT00697840

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
between 18 and 40 years old.
boolean
C0001779 (UMLS CUI [1])
written informed consent
Item
written informed consent will have been obtained from the subjects.
boolean
C0021430 (UMLS CUI [1])
good physical condition
Item
good physical condition as established by physical examination and history taking at the time of entry.
boolean
C1142435 (UMLS CUI [1])
pregnancy
Item
female participants will avoid becoming pregnant during the study period and they will have been on a contraceptive program for at least 2 months before entry
boolean
C0032961 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pregnancy or lactation
Item
pregnancy or lactation.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Hepatitis B surface antibody
Item
positive titres for anti hbs antibody.
boolean
C0149708 (UMLS CUI [1])
Hepatitis B vaccination
Item
any vaccination against hepatitis b in the past.
boolean
C0474232 (UMLS CUI [1])
mpl administration
Item
any previous administration of mpl.
boolean
C0066776 (UMLS CUI [1])
elevated serum liver enzymes
Item
elevated serum liver enzymes.
boolean
C1287351 (UMLS CUI [1])
hematologic, hepatic, renal, cardiac or respiratory disease
Item
history of significant and persisting hematologic, hepatic, renal, cardiac or respiratory disease.
boolean
C0009488 (UMLS CUI [1])
axillary temperature
Item
axillary temperature > 37.5°c at the time of injection.
boolean
C1531924 (UMLS CUI [1])
any acute disease
Item
any acute disease at the moment of entry.
boolean
C0009488 (UMLS CUI [1])
chronic alcohol consumption
Item
chronic alcohol consumption.
boolean
C0038586 (UMLS CUI [1])
immunosuppressive or immunostimulant
Item
any treatment with immunosuppressive or immunostimulant therapy.
boolean
C0021079 (UMLS CUI [1])
C0001551 (UMLS CUI [2])
drug treatment precluding inclustion into study
Item
any chronic drug treatment, which in the investigator's opinion, precludes inclusion into the study.
boolean
C0013216 (UMLS CUI [1])
C1321605 (UMLS CUI [2])
hypersensitivitiy to vaccine
Item
history of allergic disease likely to be stimulated by any component of the vaccine.
boolean
C0020517 (UMLS CUI [1,1])
C1521826 (UMLS CUI [1,2])
simultaneous administration of any other vaccines
Item
simultaneous administration of any other vaccine(s).
boolean
C1321605 (UMLS CUI [1])
administration of any immunoglobulin
Item
administration of any immunoglobulin during the study period.
boolean
C1321605 (UMLS CUI [1])
study participation status
Item
simultaneous participation in any other clinical trial.
boolean
C2348568 (UMLS CUI [1])

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