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 @ 1:40 AM
Ignite Modification Date:
2025-12-25 @ 11:56 PM
NCT ID:
NCT00780494
Group ID:
EG000
Title:
Bevacizumab+ Carboplatin +Capecitabine
Description:
Participants receive bevacizumab 15 mg/kg intravenously followed by carboplatin AUC 6 intravenously on Day 1 of a 21-day cycle, concurrently with capecitabine 850 mg/m2 twice-daily by mouth on Cycle Days 1-to-14, followed by a 1-week break.
Deaths Number Affected:
31
Deaths Number At Risk:
None
Serious Number Affected:
35
Serious Number At Risk:
35
Other Number Affected:
35
Other Number At Risk:
35
Study:
NCT00780494
Results Section:
NCT00780494
Adverse Events Module:
NCT00780494