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:
2025-12-25 @ 4:07 AM
Ignite Modification Date:
2025-12-26 @ 3:04 AM
NCT ID:
NCT00003820
Group ID:
EG000
Title:
Rituximab 375 mg/m2 Per Week
Description:
Rituximab 375 mg/m2 week by IV infusion for 4 consecutive weeks, every 6 months for 2 years.
This was a single-arm study with multiple treatment periods added by amendment (ie, Secondary Group), with results reported by treatment period. As this was always considered a single-arm study, there was no intent to report the results for the initial treatment period separately as the Initial Group vs the Secondary Group.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
28
Serious Number At Risk:
39
Other Number Affected:
39
Other Number At Risk:
39
Study:
NCT00003820
Results Section:
NCT00003820
Adverse Events Module:
NCT00003820