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 @ 6:27 PM
Ignite Modification Date:
2025-12-25 @ 3:57 PM
NCT ID:
NCT04036968
Group ID:
EG000
Title:
Placebo+Placebo
Description:
Within-subject double-blind, double-dummy administration of placebo + placebo. Order of dose randomized session days 2-5.
Within-subject test of blinded study medications: Within-subject double-blind, double-dummy, study design wherein all participants received all doses in 8-hour outpatient sessions. Primary outcomes assessed during 8-hour outpatient sessions and included laboratory pain testing, subjective reports of drug effects, and cognitive performance, evaluated as a function of study medication condition.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
31
Other Number Affected:
8
Other Number At Risk:
31
Study:
NCT04036968
Results Section:
NCT04036968
Adverse Events Module:
NCT04036968