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 investigation is to confirm the ADR development and the contributing factors possibly having an impact on the safety under the post-marketing actual use of Oxis 9 mcg Turbuhaler.

Oxis 9mcg Turbuhaler Clinical Experience Investigation

Official Title

Medical condition

Phase

Healthy volunteers

Study drug

Sex

Actual Enrollment

Study type

Age

Date

Study design

Verification:

Sponsors

Collaborators

Inclusion Criteria

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Documents available

CSR Synopsis

https://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=471&filename=D5127L00001_Oxis_Protocol_redacted.pdf

Trial Results Summaries

Contacts

Contact

Investigators

Principal Investigator