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 @ 10:02 PM
Ignite Modification Date:
2025-12-25 @ 7:38 PM
NCT ID:
NCT03188432
Group ID:
EG000
Title:
Treatment - Carboplatin, CRS, HIPEC
Description:
Beginning 4-8 weeks after completion of chemotherapy, patients undergo CRS. Patients then receive carboplatin IP over 90 minutes immediately following CRS.
Carboplatin: Given IV and IP
Quality-of-Life Assessment: Ancillary studies
Questionnaire Administration: Ancillary studies
Cytoreductive Surgery: Undergo CRS
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
27
Serious Number At Risk:
41
Other Number Affected:
41
Other Number At Risk:
41
Study:
NCT03188432
Results Section:
NCT03188432
Adverse Events Module:
NCT03188432