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 @ 5:48 PM
Ignite Modification Date:
2025-12-25 @ 3:15 PM
NCT ID:
NCT01096368
Group ID:
EG002
Title:
Arm III: Randomized to Radiation Only
Description:
Patients with supratentorial ependymoma (Grade II without GTR1 or ST Grade III) or any infratentorial ependymoma (Grade II or III) who have undergone gross or near total resection or achieved CR either after first or second resection or after post-operative induction chemotherapy are randomized to undergo conformal radiotherapy over 6-7 weeks and then undergo observation.
Deaths Number Affected:
27
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
161
Other Number Affected:
10
Other Number At Risk:
161
Study:
NCT01096368
Results Section:
NCT01096368
Adverse Events Module:
NCT01096368