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 @ 11:35 PM
Ignite Modification Date:
2025-12-25 @ 9:24 PM
NCT ID:
NCT02054156
Group ID:
EG001
Title:
Placebo
Description:
placebo and tobramycin solution for inhalation (TIS) Placebo 3 times weekly, oral suspension, volume-matched to azithromycin, for 18 months Tobramycin solution for inhalation (TIS), 300 mg, twice daily for 28 days when respiratory cultures are found positive for Pa at study visits for 18 months
placebo: 3 times weekly, oral suspension, volume-matched to azithromycin, for 18 months
Tobramycin solution for inhalation: 300 mg, twice daily for 28 days when respiratory cultures are found positive for Pa at study visits for 18 months
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
28
Serious Number At Risk:
111
Other Number Affected:
92
Other Number At Risk:
111
Study:
NCT02054156
Results Section:
NCT02054156
Adverse Events Module:
NCT02054156