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

Cross-sectional, one visit study. All the data will be collected through questionnaires. Descriptives statistics will be applied to the data. 832 patients will participate to the study and 104 physicians.

Opinion of patients under treatment that meets the criteria of new treatment strategy according to GINA 2006 - EPAGGELIA

Official Title

Medical condition

Phase

Healthy volunteers

Study drug

Sex

Actual Enrollment

Study type

Age

Date

Study design

Verification:

Sponsors

Collaborators

Inclusion Criteria

Exclusion Criteria

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Documents available

https://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_6111&studyid=1053&filename=CSR-NIS-RGR-DUM-2008-1.pdf

CSR-NIS-RGR-DUM-2008-1.pdf

CSR-NIS-RGR-DUM-2008-1.pdf

Trial Results Summaries

Contacts

Contact

Investigators

Principal Investigator