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Clinical Trials/NCT01713075
NCT01713075
Completed
Not Applicable

Symbicort Turbuhaler 30/60 Special Clinical Experience Investigation for Long-term Use for COPD Patients

AstraZeneca1 site in 1 country1,183 target enrollmentNovember 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
AstraZeneca
Enrollment
1183
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 and efficacy in long-term use of Symbicort Turbuhaler in patients with Chronic obstructive pulmonary disease (COPD) under the post-marketing actual use.

Detailed Description

Symbicort Turbuhaler 30/60 Special Clinical Experience Investigation for long-term use for COPD patients

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

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Among patients treated with Symbicort Turbuhaler due to chronic obstructive pulmonary disease(COPD), those who received the drug for the first time.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Adverse event incidence

Time Frame: 1 year

Secondary Outcomes

  • Clinical questionnaire about chronic obstructive pulmonary disease(CCQ)(At baseline, Week 12, Week 26, 1 year)

Study Sites (1)

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