ID
33061
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
Parotid / Salivary Gland Swelling AE Form
- StudyEvent: ODM
Description
Parotid/Salivary Gland Swelling Events
Description
Further Details (For GSK)
Description
Saliva Sample
Description
Event Number
Data type
integer
Description
Has a saliva sample been taken for mumps virus detection, strain identification and for viral culture?
Data type
boolean
Description
If Yes, record date
Data type
date
Description
Relationship to Investigational products
Description
Outcome
Similar models
Parotid / Salivary Gland Swelling AE Form
- StudyEvent: ODM
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