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 @ 3:00 AM
Ignite Modification Date:
2025-12-26 @ 1:40 AM
NCT ID:
NCT02311933
Group ID:
EG000
Title:
Arm I (Z-endoxifen Hydrochloride)
Description:
Patients receive 80 mg z-endoxifen hydrochloride PO on days 1-21. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
41
Other Number Affected:
34
Other Number At Risk:
41
Study:
NCT02311933
Results Section:
NCT02311933
Adverse Events Module:
NCT02311933