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 @ 2:48 PM
Ignite Modification Date:
2025-12-25 @ 1:16 PM
NCT ID:
NCT00619359
Group ID:
EG001
Title:
Aprepitant
Description:
Aprepitant 125 mg by mouth (PO), ondansetron 32 mg IV, and dexamethasone 12 mg PO on Day 1, aprepitant 80 mg PO and dexamethasone 8 mg PO on Days 2 and 3, dexamethasone 8 mg PO on Day 4.
6 patients from the aprepitant regimen were randomized to the study, but discontinued before receiving study drug. These patients were excluded from the Adverse Event tables.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
157
Serious Number At Risk:
1169
Other Number Affected:
679
Other Number At Risk:
1169
Study:
NCT00619359
Results Section:
NCT00619359
Adverse Events Module:
NCT00619359