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:
EG001
Title:
Arm B (Paclitaxel + Carboplatin + Radiation + Thalidomide)
Description:
Experimental arm. Thalidomide: daily, patients begin with 200 mg thalidomide PO as a single dose at bedtime. The dose is then increased by 100 mg every week as tolerated up to a total dose of 1000 mg; low dose aspirin: 81mg PO daily.
Paclitaxel, carboplatin and radiation same as active comparator.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
249
Serious Number At Risk:
288
Other Number Affected:
284
Other Number At Risk:
288
Study:
NCT00004859
Results Section:
NCT00004859
Adverse Events Module:
NCT00004859