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:
EG005
Title:
Arm VI (8-21 Years of Age, SDCSI, PFRT)
Description:
See Detailed Description (Arm VI)
Cisplatin: Given IV
Craniospinal Irradiation: Undergo craniospinal Irradiation
Cyclophosphamide: Given IV
Laboratory Biomarker Analysis: Correlative studies
Lomustine: Given orally
Quality-of-Life Assessment: Ancillary studies
Radiation Therapy: Undergo standard volume boost (whole posterior fossa radiation therapy)
Vincristine Sulfate: Given IV
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
18
Serious Number At Risk:
138
Other Number Affected:
135
Other Number At Risk:
138
Study:
NCT00085735
Results Section:
NCT00085735
Adverse Events Module:
NCT00085735