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 @ 4:27 AM
Ignite Modification Date:
2025-12-26 @ 3:30 AM
NCT ID:
NCT00382720
Group ID:
EG002
Title:
(TEX) Taxotere, Eloxatin and Xeloda
Description:
Participants administered Docetaxel (Taxotere) 50 mg/m² as a 1-hour intravenous (IV) infusion on day 1, Oxaliplatin (Eloxatin) 100 mg/m² as a two to six-hour IV infusion on day 1, Capecitabine (Xeloda) 625 mg/m2 two times a day continuously per chemotherapy cycle.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
36
Serious Number At Risk:
82
Other Number Affected:
77
Other Number At Risk:
82
Study:
NCT00382720
Results Section:
NCT00382720
Adverse Events Module:
NCT00382720