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 @ 7:56 PM
Ignite Modification Date:
2025-12-25 @ 5:31 PM
NCT ID:
NCT00442104
Group ID:
EG000
Title:
Ganaxolone
Description:
Participants were administered a maximum dose of 54 mg/kg/day ganaxolone oral suspension. The investigator could adjust (increase or decrease) the dose of ganaxolone by 3 mg/kg t.i.d. (total daily dose adjustment = 9 mg/kg) until the optimal dose for efficacy and tolerability was achieved.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
24
Serious Number At Risk:
54
Other Number Affected:
47
Other Number At Risk:
54
Study:
NCT00442104
Results Section:
NCT00442104
Adverse Events Module:
NCT00442104