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 @ 1:40 AM
Ignite Modification Date:
2025-12-25 @ 11:56 PM
NCT ID:
NCT01898494
Group ID:
EG004
Title:
Arm D (Cisplatin + IMRT 66 Gy)
Description:
High risk patients receive IMRT at 66 Gy QD for 33 fractions. Patients also receive cisplatin intravenously (IV) over 60 minutes on days 1, 8, 15, 22, 29, 36, and 43 during radiation therapy.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
81
Serious Number At Risk:
134
Other Number Affected:
96
Other Number At Risk:
134
Study:
NCT01898494
Results Section:
NCT01898494
Adverse Events Module:
NCT01898494