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:
2025-12-26 @ 1:19 PM
Ignite Modification Date:
2025-12-26 @ 1:19 PM
NCT ID:
NCT03865706
Group ID:
EG000
Title:
Placebo
Description:
Critically ill adults who are receiving broad-spectrum antibiotics will also receive placebo oral suspension for a minimum of 7 days.
Placebo Oral Suspension: 250cc sterile water alone, given twice daily a sweetener is added to the water to create identical flavor
Broad-spectrum antibiotics: Standard of care treatment for infections
Deaths Number Affected:
7
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
30
Other Number Affected:
15
Other Number At Risk:
30
Study:
NCT03865706
Results Section:
NCT03865706
Adverse Events Module:
NCT03865706