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 @ 4:51 PM
Ignite Modification Date:
2025-12-25 @ 2:35 PM
NCT ID:
NCT00593450
Group ID:
EG000
Title:
1-Lucentis Monthly
Description:
Lucentis® on a fixed schedule of every 4 weeks for 1 year; at 1 year, re-randomization to Lucentis® every 4 weeks or to variable dosing.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
53
Serious Number At Risk:
301
Other Number Affected:
3
Other Number At Risk:
301
Study:
NCT00593450
Results Section:
NCT00593450
Adverse Events Module:
NCT00593450