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 @ 1:52 PM
Ignite Modification Date:
2025-12-25 @ 12:42 PM
NCT ID:
NCT00505895
Group ID:
EG000
Title:
Fludarabine + Melphalan + Stem Cell Infusion
Description:
Fludarabine 30 mg/m\^2 intravenous (IV) daily over 30 minutes for 4 Days (Beginning Day -4).
Melphalan 140 mg/m\^2 IV over 20 minutes on Day -1. Stem Cell Infusion on Day 0. Rituximab 375 mg/m\^2 IV infused starting on day -5.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
23
Serious Number At Risk:
27
Other Number Affected:
8
Other Number At Risk:
27
Study:
NCT00505895
Results Section:
NCT00505895
Adverse Events Module:
NCT00505895