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:
2025-12-26 @ 10:58 AM
Ignite Modification Date:
2025-12-26 @ 10:58 AM
NCT ID:
NCT02343406
Group ID:
EG002
Title:
Control_lomustine
Description:
Adult subjects relapsing during temozolomide (TMZ) treatment or within the first 16 weeks after the first day of the last TMZ cycle received lomustine on Day 1 of every 42-day treatment period until one of the treatment withdrawal criteria was met, up to a maximum of 1 year.
Deaths Number Affected:
52
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
56
Other Number Affected:
46
Other Number At Risk:
56
Study:
NCT02343406
Results Section:
NCT02343406
Adverse Events Module:
NCT02343406