Be SMART NIS, Moderate to Servere Asthma Patient Observation
1 other identifier
observational
900
1 country
1
Brief Summary
Screen for moderate to severe asthma patients with suboptimal asthma control (as defined by GINA-Guidelines). Document current asthma control status. Re-evaluate asthma therapy and document new therapy if applicable.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 9, 2007
CompletedFirst Posted
Study publicly available on registry
August 10, 2007
CompletedMarch 27, 2009
March 1, 2009
August 9, 2007
March 26, 2009
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Moderate to severe asthma with suboptimal control
You may not qualify if:
- Intermittent or mild asthma, patient with good asthma control
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- AstraZenecalead
Study Sites (1)
Research Site
Vienna, Austria
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Wolfgang Pohl, PHD
Executive Board OGP (Austria Society of Pneumology
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
August 9, 2007
First Posted
August 10, 2007
Last Updated
March 27, 2009
Record last verified: 2009-03