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 @ 3:03 AM
Ignite Modification Date:
2025-12-26 @ 1:43 AM
NCT ID:
NCT02166333
Group ID:
EG002
Title:
Those With Experience on 1000 IU
Description:
This group includes those randomized to 1000 IU and 96 participants randomized to 2000 or 4000 who were issued at least 1 bottle of 1000 IU. Note that participants who switched doses during the trial may have an event while in their original group as well as in the 1000 group if the event recurred after switching to 1000 IU.
Deaths Number Affected:
4
Deaths Number At Risk:
None
Serious Number Affected:
49
Serious Number At Risk:
308
Other Number Affected:
250
Other Number At Risk:
308
Study:
NCT02166333
Results Section:
NCT02166333
Adverse Events Module:
NCT02166333