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 @ 4:49 AM
Ignite Modification Date:
2025-12-26 @ 3:50 AM
NCT ID:
NCT00114218
Group ID:
EG000
Title:
Treatment (Gemcitabine Hydrochloride, Docetaxel)
Description:
Patients receive gemcitabine IV over 30 minutes followed by docetaxel IV over 1 hour on days 1, 8, and 15. Courses repeat every 28 days in the absence of unacceptable toxicity or disease progression.
Gemcitabine Hydrochloride: Given IV
Docetaxel: Given IV
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
11
Serious Number At Risk:
24
Other Number Affected:
22
Other Number At Risk:
24
Study:
NCT00114218
Results Section:
NCT00114218
Adverse Events Module:
NCT00114218