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 @ 12:36 AM
Ignite Modification Date:
2025-12-25 @ 10:45 PM
NCT ID:
NCT03349567
Group ID:
EG001
Title:
Patients Seen at Control ED Sites During the Intervention Period
Description:
All patients seen in the EDs designated as control sites will be considered to have been part of the control group. For this adverse event reporting section, we are reporting ED patient-visits during the intervention period at control sites.
Because this study was not randomized, a more accurate assessment of adverse events would require a difference-in-differences analysis across the baseline and intervention periods while controlling for baseline differences between intervention and control sites. Such an analysis is described in our statistical analysis plan and will be reported in our published paper.
Deaths Number Affected:
176
Deaths Number At Risk:
None
Serious Number Affected:
1863
Serious Number At Risk:
28835
Other Number Affected:
27
Other Number At Risk:
28835
Study:
NCT03349567
Results Section:
NCT03349567
Adverse Events Module:
NCT03349567