Description:

Phase A - Year 2 Extension - Telephone contact 28 - GSK Study: Evaluation of safety and efficacy of VarilrixTM and of Combined Measles-Mumps-Rubella-Varicella Vaccine NCT00226499 Study ID: 100388 Clinical Study ID: 100388 Study Title: Study in Healthy Children (<2 Years) to Evaluate the Safety and Efficacy of GSK Biologicals' Live Attenuated Varicella Vaccine (VarilrixTM) and of GSK Biologicals' Combined Measles-Mumps-Rubella-Varicella Vaccine Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00226499 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: Varicella Vaccine Trade Name: BIO OKAH; Varilrix Study Indication: Varicella

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Versions (1) ▾
  1. 9/2/17
Copyright Holder:
glaxoSmithKline
Uploaded on:

September 2, 2017

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License:
Creative Commons BY-NC 3.0
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Phase A - Year 2 Extension - Telephone contact 28 - GSK Study: Evaluation of safety and efficacy of VarilrixTM and of Combined Measles-Mumps-Rubella-Varicella Vaccine NCT00226499

Phase A - Year 2 Extension - Telephone contact 28 - GSK Study: Evaluation of safety and efficacy of VarilrixTM and of Combined Measles-Mumps-Rubella-Varicella Vaccine NCT00226499

Subject's contact
Was the subject successfully contacted at scheduled Telephone Contact 28?
Has the subject been seen or contacted between the previous contact and this contact?
Household exposure
Irrespective of whether the subject developed/develops varicella/zoster, was the subject exposed for more than one day to any varicella or zoster case presented by a household member or another person living temporarily within the household between the previous contact and this contact?
Household exposure number
Type of exposure
Varicella or zoster
Did the subject present any signs of varicella or zoster symptoms between the previous contact and this contact?
Serious adverse event
Did the subject experience any serious adverse event between the previous contact and this contact?