ID
33929
Beschreibung
Study ID:103860/269 Clinical Study ID:103860/269 (HBV-269) Study Title: Phase II study to evaluate the immunogenicity of GSK Biologicals' preservative-free Engerix-B and thiomersal-free Engerix-B vaccines compared to Engerix™-B and evaluate safety and reactogenicity of each vaccine when administered intramuscularly according to a 0, 1, 6 month schedule in healthy volunteers Patient Level Data:Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 2 Study Recruitment Status: Completed Generic Name: Hepatitis B Vaccine, Recombinant Trade Name: Engerix-B Study Indication: Hepatitis B
Stichworte
Versionen (1)
- 08.01.19 08.01.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
8. Januar 2019
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Immunogenicity, safety and reactogenicity of preservative-free Engerix-B and thiomersal-free Engerix-B vaccines compared to Engerix™️-B
Serious Adverse Events
- StudyEvent: ODM
Beschreibung
Subject Demography
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C1704791
Beschreibung
Adverse Event
Alias
- UMLS CUI-1
- C1519255
Beschreibung
Serious Adverse Event, Diagnosis
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0011900
Beschreibung
Serious Adverse Event, Start Date, Start Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C1301880
Beschreibung
Serious Adverse Event, Symptom intensity
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
Beschreibung
Serious Adverse Event, Relationship, Vaccines
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0042210
Beschreibung
Serious Adverse Event, Adverse Event Outcome
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1705586
Beschreibung
Serious Adverse Event, Action taken with study
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2826626
- UMLS CUI [1,2]
- C0042210
Beschreibung
Serious Adverse Event, Vaccination, Continuous, Event
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0042196
- UMLS CUI [1,3]
- C0549178
- UMLS CUI [1,4]
- C0441471
Beschreibung
Serious Adverse Event, Criteria
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0243161
Beschreibung
Event, Other
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0441471
- UMLS CUI [1,2]
- C0205394
Beschreibung
Serious Adverse Event, Etiology aspects
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0015127
Beschreibung
Serious Adverse Event, Withdraw
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2349954
Beschreibung
Study vaccine information
Alias
- UMLS CUI-1
- C0042210
- UMLS CUI-2
- C0304229
- UMLS CUI-3
- C1533716
Beschreibung
Vaccines, Experimental
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0042210
- UMLS CUI [1,2]
- C0304229
Beschreibung
Vaccines, Dose, Number
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0042210
- UMLS CUI [1,2]
- C1115464
Beschreibung
Vaccines, Lot Number
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0042210
- UMLS CUI [1,2]
- C1115660
Beschreibung
Vaccines, Drug Administration Routes, Anatomical Site
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0042210
- UMLS CUI [1,2]
- C0013153
- UMLS CUI [1,3]
- C1515974
Beschreibung
Vaccines, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0042210
- UMLS CUI [1,2]
- C0011008
Beschreibung
Concomitant medication / vaccination that could have contributed to this SAE
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2347852
Beschreibung
Serious Adverse Event, Concomitant Agent
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
Beschreibung
Serious Adverse Event, Concomitant Agent, Medication dose
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C3174092
Beschreibung
Serious Adverse Event, Concomitant Agent, Frequencies
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0439603
Beschreibung
Serious Adverse Event, Concomitant Agent, Drug Administration Routes
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0013153
Beschreibung
Serious Adverse Event, Concomitant Agent, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0808070
Beschreibung
Serious Adverse Event, Concomitant Agent, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0806020
Beschreibung
Relevant intercurrent illness & medical history hat could have contributed to this SAE
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0012634
Beschreibung
Drug(s) used to treat this SAE
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0013227
Beschreibung
Serious Adverse Event, Pharmaceutical Preparations
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013227
Beschreibung
Serious Adverse Event, Pharmaceutical Preparations, Dosage
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0178602
Beschreibung
Serious Adverse Event, Pharmaceutical Preparations, Frequencies
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0439603
Beschreibung
Serious Adverse Event, Pharmaceutical Preparations, Drug Administration Routes
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0013153
Beschreibung
Serious Adverse Event, Pharmaceutical Preparations, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0808070
Beschreibung
Serious Adverse Event, Pharmaceutical Preparations, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0806020
Beschreibung
Surgical treatment for this SAE
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0543467
Beschreibung
Description
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0678257
Beschreibung
Investigator signature
Alias
- UMLS CUI-1
- C2346576
Beschreibung
Investigator Signature
Datentyp
text
Alias
- UMLS CUI [1]
- C2346576
Beschreibung
Investigator Signature, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Beschreibung
Investigator Name
Datentyp
text
Alias
- UMLS CUI [1]
- C2826892
Beschreibung
Comments
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0947611
Beschreibung
Investigator signature
Alias
- UMLS CUI-1
- C2346576
Beschreibung
Investigator Signature
Datentyp
text
Alias
- UMLS CUI [1]
- C2346576
Beschreibung
Investigator Signature, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Beschreibung
Investigator Name
Datentyp
text
Alias
- UMLS CUI [1]
- C2826892
Ähnliche Modelle
Serious Adverse Events
- StudyEvent: ODM
C1704791 (UMLS CUI-2)
C0011900 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
C0518690 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,2])
C0042210 (UMLS CUI [1,3])
C1705586 (UMLS CUI [1,2])
C0042210 (UMLS CUI [1,2])
C0042196 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
C0441471 (UMLS CUI [1,4])
C0243161 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,2])
C0304229 (UMLS CUI-2)
C1533716 (UMLS CUI-3)
C0304229 (UMLS CUI [1,2])
C1115464 (UMLS CUI [1,2])
C1115660 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C2347852 (UMLS CUI-2)
C2347852 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0012634 (UMLS CUI-2)
C0012634 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C0150312 (UMLS CUI [1,3])
C0013227 (UMLS CUI-2)
C0013227 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0543467 (UMLS CUI-2)
C0543467 (UMLS CUI [1,2])
C0678257 (UMLS CUI-2)
C0678257 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])