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 @ 2:30 AM
Ignite Modification Date:
2025-12-26 @ 1:05 AM
NCT ID:
NCT01302834
Group ID:
EG000
Title:
IMRT + Cisplatin
Description:
Intensity-modulated radiotherapy (IMRT) with concurrent cisplatin
Cisplatin: 100 mg/m2 IV on days 1 and 22 of IMRT
IMRT: 35 fractions over 6 weeks, 6 fractions per week, 2 Gray per fraction to total dose of 70 Gy.
Deaths Number Affected:
64
Deaths Number At Risk:
None
Serious Number Affected:
177
Serious Number At Risk:
398
Other Number Affected:
398
Other Number At Risk:
398
Study:
NCT01302834
Results Section:
NCT01302834
Adverse Events Module:
NCT01302834