Symbicort Turbuhaler 30/60 Clinical Experience Investigation

NCT01232348 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3643

Last updated 2011-12-07

No results posted yet for this study

Summary

The purpose of this study is to confirm the safety (ADR related to beta stimulant drugs, unexpected ADRs) and efficacy of Symbicort in daily practice and the control status on bronchial asthma and Patient satisfaction

Conditions

  • Bronchial Asthma

Sponsors & Collaborators

Principal Investigators

  • Yoshida Shigeru, MD · AstraZeneca

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2011-10-31
Completion
2011-10-31

Countries

  • Japan

Study Locations

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Entities

Companies

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 NCT01232348 on ClinicalTrials.gov