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 @ 10:30 PM
Ignite Modification Date:
2025-12-25 @ 8:03 PM
NCT ID:
NCT02766335
Group ID:
EG001
Title:
Arm II (Docetaxel - Closed to Accrual 4/2015)
Description:
Participants receive docetaxel IV on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. (closed to accrual with Revision #2 4/22/15)
Docetaxel: Given IV
Laboratory Biomarker Analysis: Correlative studies
Deaths Number Affected:
26
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
30
Other Number Affected:
30
Other Number At Risk:
30
Study:
NCT02766335
Results Section:
NCT02766335
Adverse Events Module:
NCT02766335