Pulmicort Respules 0.25/0.5 Specific Clinical Experience Investigation

NCT01232322 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 633

Last updated 2013-01-24

No results posted yet for this study

Summary

The purpose of this study is to investigate the safety and efficacy for long term treatment of the drug in children aged 6 months and \< 5 years on bronchial asthma in daily clinical usage.

Conditions

  • Bronchial Asthma

Sponsors & Collaborators

Principal Investigators

  • Yoshida Shigeru, MD · AstraZeneca

Eligibility

Min Age
6 Months
Max Age
5 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-10-31
Primary Completion
2011-07-31
Completion
2011-07-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01232322 on ClinicalTrials.gov