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 @ 2:09 AM
Ignite Modification Date:
2025-12-26 @ 12:36 AM
NCT ID:
NCT01412060
Group ID:
EG000
Title:
Cariprazine - Open-label Phase
Description:
Participants received 3, 6, or 9 mg cariprazine orally once a day for 6 weeks; the dose could be modified during this time. The cariprazine dose was fixed at 3, 6, or 9 mg for the last 14 weeks of this 20 week Open-label Phase.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
50
Serious Number At Risk:
765
Other Number Affected:
425
Other Number At Risk:
765
Study:
NCT01412060
Results Section:
NCT01412060
Adverse Events Module:
NCT01412060