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
ConditionsBronchial Asthma
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
Investigators
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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