Twice-daily budesonide inhalation suspension in infants and children < 4 and > or = 4 years of age with persistent asthma

J Asthma. 2002 May;39(3):227-37. doi: 10.1081/jas-120002472.

Abstract

A retrospective analysis, based on a randomized, placebo-controlled, 12-week study in children 6 months to 8 years of age with persistent asthma, was performed to compare the efficacy and safety of budesonide inhalation suspension 0.25 mg and 0.5 mg twice daily vs. placebo in children < 4 and > or = 4 years of age. Both age groups demonstrated significant (p < or = 0.050) improvement in nighttime and daytime asthma symptom scores and decreased bronchodilator use compared with placebo. In addition, the safety profile of twice-daily budesonide inhalation suspension was favorable in both age groups.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Inhalation
  • Asthma / drug therapy*
  • Bronchodilator Agents / therapeutic use*
  • Budesonide / administration & dosage*
  • Child, Preschool
  • Drug Administration Schedule
  • Female
  • Humans
  • Infant
  • Male
  • Randomized Controlled Trials as Topic
  • Retrospective Studies

Substances

  • Bronchodilator Agents
  • Budesonide