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 @ 3:34 PM
Ignite Modification Date:
2025-12-25 @ 1:47 PM
NCT ID:
NCT06363292
Group ID:
EG000
Title:
PRO-231
Description:
* PRO-231: Moxifloxacin 0.5% Ophthalmic solution.
* Dosage: 1 drop every 6 hours (3 daily applications \[TID\], in the right eye).
* Route of administration: Topical ophthalmic.
PRO-231: Moxifloxacin 0.5% Ophthalmic solution.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
18
Other Number Affected:
3
Other Number At Risk:
18
Study:
NCT06363292
Results Section:
NCT06363292
Adverse Events Module:
NCT06363292