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Clinical Trials/NCT01711840
NCT01711840
Completed
N/A

Symbicort Turbuhaler 30/60 Clinical Experience Investigation for Treatment With Symbicort as Maintenance Therapy and as Needed in Response to Symptoms

AstraZeneca1 site in 1 country2,409 target enrollmentNovember 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Bronchial Asthma
Sponsor
AstraZeneca
Enrollment
2409
Locations
1
Primary Endpoint
Adverse event incidence
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of the investigation is to confirm the safety of patients receiving Symbicort Turbuhaler as maintenance and reliever therapy ( Symbicort SMART) under the post-marketing actual use.

Detailed Description

Symbicort Turbuhaler 30/60 Clinical Experience Investigation for treatment with Symbicort as maintenance therapy and as needed in response to symptoms

Registry
clinicaltrials.gov
Start Date
November 2012
End Date
August 2015
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients receiving Symbicort Turbuhaler as maintenance and reliever therapy for the first time due to 'bronchial asthma ',and possibly requiring as-needed inhalations during the observation period

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Adverse event incidence

Time Frame: 12 weeks

Study Sites (1)

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