Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 2:08 PM
Ignite Modification Date:
2025-12-25 @ 12:49 PM
NCT ID:
NCT00975195
Group ID:
EG000
Title:
Fluticasone Maintenance
Description:
18μg tiotropium administered by oral inhalation once daily (q.d.), 50μg salmeterol and 500μg fluticasone, each administered by oral inhalation twice daily (b.i.d) for 6 weeks (open-label run in period), followed by 18 μg tiotropium q.d., 50 μg salmeterol b.i.d.,and 500 μg fluticasone b.i.d. for 52 weeks (randomised treatment period).
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
292
Serious Number At Risk:
1243
Other Number Affected:
464
Other Number At Risk:
1243
Study:
NCT00975195
Results Section:
NCT00975195
Adverse Events Module:
NCT00975195