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 @ 2:39 PM
Ignite Modification Date:
2025-12-25 @ 1:11 PM
NCT ID:
NCT00004859
Group ID:
EG000
Title:
Arm A (Paclitaxel + Carboplatin + Radiation )
Description:
Active comparator. Induction dosing: Paclitaxel, 225 mg/m²; Carboplatin, AUC=6.0. Concurrent dosing: Paclitaxel, 45 mg/m2; Carboplatin: AUC=2.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
222
Serious Number At Risk:
289
Other Number Affected:
283
Other Number At Risk:
289
Study:
NCT00004859
Results Section:
NCT00004859
Adverse Events Module:
NCT00004859