ID
23899
Beschrijving
Study part: Study Conclusion. A phase 2 study to assess safety, reactogenicity and immunogenicity of a booster dose of an investigational vaccination regimen and GSK Biologicals Hib-MenC vaccine (co-administered with Infanrix penta) compared to a booster dose of Menjugate (co-administered with Infanrix hexa).Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Study ID: 100381, Clinical Study ID: 100381
Trefwoorden
Versies (1)
- 17-07-17 17-07-17 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
17 juli 2017
DOI
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Licentie
Creative Commons BY-NC 3.0
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Study Conclusion Hib-MenCY-TT-004 BST 003 Neisseria Meningitidis-Haemophilus influenzae type b Vaccine 100381
Study Conclusion
- StudyEvent: ODM
Beschrijving
STATUS OF TREATMENT BLIND
Alias
- UMLS CUI-1
- C2347797
- UMLS CUI-2
- C0039798
- UMLS CUI-3
- C2347038
Beschrijving
Blinded Clinical Study
Datatype
boolean
Alias
- UMLS CUI [1]
- C2347038
Beschrijving
date
Datatype
date
Alias
- UMLS CUI [1]
- C0011008
Beschrijving
reason
Datatype
text
Alias
- UMLS CUI [1]
- C0392360
Beschrijving
Other
Datatype
text
Alias
- UMLS CUI [1]
- C0205394
Beschrijving
ELIMINATION CRITERIA
Alias
- UMLS CUI-1
- C0680251
Beschrijving
STUDY CONCLUSION
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Beschrijving
study subject participation status
Datatype
boolean
Alias
- UMLS CUI [1]
- C2348568
Beschrijving
Reason
Datatype
integer
Alias
- UMLS CUI [1]
- C0392360
Beschrijving
SAE
Datatype
text
Alias
- UMLS CUI [1]
- C1519255
Beschrijving
Non-Serious adverse event
Datatype
text
Alias
- UMLS CUI [1]
- C1518404
Beschrijving
Protocol violation
Datatype
text
Alias
- UMLS CUI [1]
- C1709750
Beschrijving
(e.g. : consent withdrawal, Protocol violation, …)
Datatype
text
Alias
- UMLS CUI [1]
- C0205394
Beschrijving
Investigator desicion study discontinuation
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0008961
- UMLS CUI [1,2]
- C0679006
- UMLS CUI [1,3]
- C2826233
Beschrijving
Parents desicion study discontinuation
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0030551
- UMLS CUI [1,2]
- C0679006
- UMLS CUI [1,3]
- C2826233
Beschrijving
Date of last contact
Datatype
date
Alias
- UMLS CUI [1]
- C0805839
Beschrijving
medical condition contact last
Datatype
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0332158
- UMLS CUI [1,3]
- C1517741
Beschrijving
INVESTIGATOR'S SIGNATURE
Alias
- UMLS CUI-1
- C2346576
Beschrijving
confirmation
Datatype
boolean
Alias
- UMLS CUI [1]
- C0750484
Beschrijving
Investigators signature
Datatype
text
Alias
- UMLS CUI [1]
- C2346576
Beschrijving
Investigator name
Datatype
text
Alias
- UMLS CUI [1]
- C2826892
Beschrijving
Date
Datatype
date
Alias
- UMLS CUI [1]
- C0011008
Similar models
Study Conclusion
- StudyEvent: ODM
C1519255 (UMLS CUI [1,2])
C0039798 (UMLS CUI-2)
C2347038 (UMLS CUI-3)
C0679006 (UMLS CUI [1,2])
C2826233 (UMLS CUI [1,3])
C0679006 (UMLS CUI [1,2])
C2826233 (UMLS CUI [1,3])
C0332158 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])