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 @ 6:50 PM
Ignite Modification Date:
2025-12-25 @ 4:21 PM
NCT ID:
NCT00942357
Group ID:
EG001
Title:
Arm II (Paclitaxel and Carboplatin)
Description:
Patients receive paclitaxel IV over 3 hours and carboplatin IV on day 1. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity.
Carboplatin: Given IV
Paclitaxel: Given IV
Quality-of-Life Assessment: Ancillary studies
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
61
Serious Number At Risk:
361
Other Number Affected:
360
Other Number At Risk:
361
Study:
NCT00942357
Results Section:
NCT00942357
Adverse Events Module:
NCT00942357