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

The purpose of the study is to compare the efficacy of a flexible dose of Symbicort with conventional stepwise treatment according to asthma treatment guidelines in patients with persistent asthma

STYLE - Symbicort single inhaler therapy vs conventional therapy in treatment of persistent asthma

Research Site

Researh Site

A comparison of the efficacy of Symbicort® Single inhaler Therapy (Symbicort Turbuhaler® 160/4.5 mg 1 inhalation b.i.d. plus as-needed) and conventional best practice for the treatment of persistent asthma in adolescents and adults – a 26 weeks, randomised, open-label, parallel-group, multicentre study

STYLE - Symbicort single inhaler therapy vs conventional therapy in treatment of persistent asthma

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Documents available

http://www.astrazeneca.com/node/emailtriage.aspx

https://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_6111&studyid=528&filename=CSR-D5890L00014.pdf

CSR-D5890L00014.pdf

Trial Results Summaries

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