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 @ 11:54 PM
Ignite Modification Date:
2025-12-25 @ 9:50 PM
NCT ID:
NCT01101451
Group ID:
EG001
Title:
Arm II (Cisplatin + Radiation)
Description:
Patients receive cisplatin IV over 1-2 hours on day 1 and undergo radiotherapy as in Arm I. Treatment with cisplatin repeats every 7 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.
Deaths Number Affected:
12
Deaths Number At Risk:
None
Serious Number Affected:
9
Serious Number At Risk:
161
Other Number Affected:
158
Other Number At Risk:
161
Study:
NCT01101451
Results Section:
NCT01101451
Adverse Events Module:
NCT01101451