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 @ 4:16 PM
Ignite Modification Date:
2025-12-25 @ 2:13 PM
NCT ID:
NCT03219866
Group ID:
EG001
Title:
Dry Powder Inhaler
Description:
Subjects will receive a LABA/ICS (Advair Diskus, twice daily) plus a long-acting anticholinergic (LAMA; Spiriva Handihaler, once daily).
Dry Powder Inhaler: Patients treated and discharged on Dry Powder Inhalers
Advair Diskus: Subjects will receive a LABA/ICS (Advair Diskus, twice daily)
Spiriva HandiHaler: Subjects will receive a long-acting anticholinergic (LAMA-Spiriva Handihaler, once daily)
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
19
Other Number Affected:
0
Other Number At Risk:
19
Study:
NCT03219866
Results Section:
NCT03219866
Adverse Events Module:
NCT03219866