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 @ 2:14 PM
Ignite Modification Date:
2025-12-25 @ 12:52 PM
NCT ID:
NCT01696695
Group ID:
EG000
Title:
mCRC Participants
Description:
Newly diagnosed mCRC participants, who received first line capecitabine based chemotherapy according to effective official Summary of Product Characteristics, were observed. The choice of therapy was based on exclusively the medical decision of the treating physician before study enrollment. The study protocol did not enforce treatment initiation and also did not specify any treatment regimen.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
55
Serious Number At Risk:
882
Other Number Affected:
140
Other Number At Risk:
882
Study:
NCT01696695
Results Section:
NCT01696695
Adverse Events Module:
NCT01696695