The purpose of this study is to assess vaccine effectiveness of Rotarix in preventing rotavirus severe gastroenteritis among hospitalized infants, in Belgium.
Study Type
OBSERVATIONAL
Enrollment
643
Stool sample
GSK Investigational Site
Antwerp, Belgium
Occurrence of PCR-confirmed rotavirus (RV) severe gastroenteritis (SGE) in children fully vaccinated with Rotarix or in unvaccinated children
Time frame: More than 14 days after receipt of vaccine
Occurrence of PCR-confirmed RV SGE in children who received one or two doses of Rotarix or in unvaccinated children
Time frame: More than 14 days after receipt of vaccine
Occurrence of PCR-confirmed RV SGE in children who received at least one dose of Rotarix or Rotateq in unvaccinated children
Time frame: More than 14 days after receipt of vaccine
Occurrence of SGE due to RV among children born after 01 October 2006, at least 14 weeks of age and admitted to hospital
Time frame: Average time frame: 1 year from the date of subject enrolment
Occurrence of co-infections with other organisms among children born after 1 October 2006, at least 14 weeks of age and hospitalized with PCR-confirmed RV SGE
Time frame: Average time frame: 1 year from the date of subject enrolment
Occurrence of PCR-confirmed RV SGE by age and month of year, among children born after 01 October 2006, at least 14 weeks of age and admitted to the hospital
Time frame: Average time frame: 1 year from the date of subject enrolment
Occurrence of RV serotypes among hospitalized PCR-confirmed RV SGE children born after 01 October 2006 and at least 14 weeks of age
Time frame: Average time frame: 1 year from the date of subject enrolment
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GSK Investigational Site
Brussels, Belgium
GSK Investigational Site
Brussels, Belgium
GSK Investigational Site
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...and 19 more locations