Clinical trial

Prophylactic Antipyretic Treatment in Children Receiving Pneumococcal Conjugate…

NCT00370318 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00370318
Title Prophylactic Antipyretic Treatment in Children Receiving Pneumococcal Conjugate and Standard Infant Vaccines
Official title Multicentre Study to Assess the Effect of Prophylactic Antipyretic Treatment on the Rate of Febrile Reactions Following Concomitant Administration of GSK Biologicals' 10-valent Pneumococcal Conjugate, Infanrix Hexa and Rotarix Vaccines
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Infections, Rotavirus
Intervention type Biological, Drug
Interventions 10 valent pneumococcal conjugate vaccine, Infanrix Hexa, Rotarix, Paracetamol
Enrollment 400
Start date Sep 1, 2006
Completion Apr 1, 2007
First posted Aug 31, 2006
Last update posted Mar 23, 2017
Countries Czechia

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies