EU Clinical Trial Information System (CTIS)

Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.

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Official Title

Moderate and severe asthma patients stabilized on Symbicort SMART

The primary objective of this non-interventional study is to evaluate efficacy of Symbicort®  SMART treatment in adult patients with moderate to severe asthma using ACQ scores during 6 months period

NIS-observe treatment efficacy in maintaining symptoms control in moderate/severe asthma with Symbicort SMART

Research Site

SMART way of treating asthma. Non-interventional study to evaluate clinical efficacy of  Symbicort® Maintenance And Reliever Therapy (Symbicort® SMART) in the treatment of patients with moderate and severe asthma

NIS-observe treatment efficacy in maintaining symptoms control in moderate/severe asthma with Symbicort SMART

Official Title

Medical condition

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Healthy volunteers

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Study design

Verification:

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Inclusion Criteria

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Documents available

CSR-NIS-RRO-SYM-2008-1.pdf

CSR-NIS-RRO-SYM-2008-1.pdf

Trial Results Summaries

Contacts

Contact

Investigators

Principal Investigator