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 @ 10:20 PM
Ignite Modification Date:
2025-12-25 @ 7:53 PM
NCT ID:
NCT02784535
Group ID:
EG000
Title:
Dose Optimization Phase
Description:
-1 to -10 days Open-label, dose-optimization phase: To test two doses of Atomoxetine (10,18 mg), until they met criteria for Atomoxetine Responders.
total of 48 participated in this phase. 40 participants were qualified as Atomoxetine responders.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
48
Other Number Affected:
1
Other Number At Risk:
48
Study:
NCT02784535
Results Section:
NCT02784535
Adverse Events Module:
NCT02784535