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 @ 5:00 AM
Ignite Modification Date:
2025-12-26 @ 4:00 AM
NCT ID:
NCT04799418
Group ID:
EG001
Title:
Experimental: Active-active
Description:
This group received active (i.e. time-varying caloric vestibular stimulation) treatment with the study device in a randomized controlled trial that immediately preceded this open label extension trial during which participants received active treatment. Data obtained from this group was only utilized for exploratory outcome measures.
Treatment was \~20 minutes, 2x per day for 12 weeks, then a follow-up period without treatment for 16 weeks, then another 8 week treatment period with the active treatment.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
79
Other Number Affected:
42
Other Number At Risk:
79
Study:
NCT04799418
Results Section:
NCT04799418
Adverse Events Module:
NCT04799418