ID
33068
Description
Study ID: 104020 Clinical Study ID: 104020 Study Title: Blinded, randomised study to assess the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals’ live attenuated measles-mumps-rubella-varicella candidate vaccine when given to healthy children in their second year of life Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00126997 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Completed Generic Name: Combined Measles, Mumps, Rubella, Varicella Vaccine Trade Name: Priorix Tetra Study Indication: Measles; Mumps; Rubella; Varicella CRF Seiten: 268-336; 870-938
Keywords
Versions (1)
- 11/26/18 11/26/18 -
Copyright Holder
GSK group of companies
Uploaded on
November 26, 2018
DOI
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License
Creative Commons BY-NC 3.0
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Immunogenicity of Combined Measles, Mumps, Rubella, Varicella Vaccine for healthy 2 y.o children - 104020
Febrile Convulsions AE Form
- StudyEvent: ODM
Description
Febrile Convulsions - Suspected Signs of Meningitis
Description
Further Details (For GSK)
Description
Event Number
Data type
text
Description
Date started
Data type
date
Description
Date stopped
Data type
date
Description
Intensity
Data type
text
Description
Was a neurological examination performed?
Data type
boolean
Description
If Yes, was a lumbar puncture performed?
Data type
boolean
Description
If Yes, date of exam
Data type
date
Description
Relationship to investigational products
Data type
boolean
Description
Outcome
Data type
text
Similar models
Febrile Convulsions AE Form
- StudyEvent: ODM
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