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:
EG000
Title:
Nebulizers
Description:
Subjects will receive a long-acting B2-agonist (LABA; Brovana, twice daily), corticosteroid (ICS; Pulmicort, twice daily), and a short-acting anti-cholinergic (SAMA; Atrovent, three times a day).
Nebulizers: Patients treated and discharged on nebulized bronchodilators
Brovana: Subjects will receive a long-acting B2-agonist(LABA; Brovana, twice daily)
Pulmicort: Subjects will receive a corticosteroid (ICS; Pulmicort, twice daily)
Atrovent: Subjects will receive a short-acting anti-cholinergic (SAMA; Atrovent, three times a day)
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
21
Other Number Affected:
0
Other Number At Risk:
21
Study:
NCT03219866
Results Section:
NCT03219866
Adverse Events Module:
NCT03219866