ID
33067
Beskrivning
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
Nyckelord
Versioner (2)
- 2018-11-23 2018-11-23 -
- 2018-11-26 2018-11-26 -
Rättsinnehavare
GSK group of companies
Uppladdad den
26 november 2018
DOI
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Licens
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
Visit 2: Vaccine Administration
- StudyEvent: ODM
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Vaccine Administration
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Vaccine
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Only ONE box must be ticked by vaccine
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text
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if Replacement vial, record number
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integer
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If Wrong vial number, please record the correct one
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integer
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Side/ Site/ Route
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Administration according to Protocol
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If any adverse event soccurred during the immediate post-vaccination time (30 min) please fill in the Solicited Adverse Events section, the Non-Serious Adverse Event section or a SAE form. If any prophylactic medication has been administered -> Medication Form; If any other vaccines administered -> Concomitant Vaccination form.
Datatyp
boolean
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If No, please tick all items that apply: Side
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integer
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Site
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text
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Route
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text
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Comment
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text
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Non-administration
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Please tick ONE most appropriate category for non administration
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text
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If SAE, specify SAE Number
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integer
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If Non-SAE, please specify unsolicited AE Number
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integer
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e.g., consent withdrawal, protocol violation, etc
Datatyp
text
Beskrivning
Please tick who took the decision
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text
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Visit 2: Vaccine Administration
- StudyEvent: ODM