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 @ 10:14 PM
Ignite Modification Date:
2025-12-25 @ 7:49 PM
NCT ID:
NCT00085735
Group ID:
EG004
Title:
Arm V (8-21 Years of Age, SDCSI, IFRT)
Description:
See Detailed Description (Arm V)
Cisplatin: Given IV
Craniospinal Irradiation: Undergo craniospinal Irradiation
Cyclophosphamide: Given IV
Involved-Field Radiation Therapy: Undergo smaller volume boost (involved-field radiation therapy)
Laboratory Biomarker Analysis: Correlative studies
Lomustine: Given orally
Quality-of-Life Assessment: Ancillary studies
Vincristine Sulfate: Given IV
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
16
Serious Number At Risk:
130
Other Number Affected:
123
Other Number At Risk:
130
Study:
NCT00085735
Results Section:
NCT00085735
Adverse Events Module:
NCT00085735