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 @ 1:06 AM
Ignite Modification Date:
2025-12-25 @ 11:18 PM
NCT ID:
NCT04178993
Group ID:
EG001
Title:
Active Comparator: Duloxetine (60 mg)
Description:
Subjects will be maintained on oral duloxetine. Subjects will be maintained on duloxetine and methylphenidate during placebo maintenance. Methamphetamine will be administered acutely during duloxetine maintenance. Placebo will be administered acutely during duloxetine maintenance.
Methamphetamine: In each arm, subjects will receive doses of methamphetamine.
Methylphenidate: In each arm, subjects will receive methylphenidate capsules.
Placebo oral capsule: In each arm, subjects will receive placebo capsules.
Duloxetine: Subjects will receive duloxetine capsules in the duloxetine arm.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
4
Other Number Affected:
2
Other Number At Risk:
4
Study:
NCT04178993
Results Section:
NCT04178993
Adverse Events Module:
NCT04178993