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 @ 3:16 PM
Ignite Modification Date:
2025-12-25 @ 1:38 PM
NCT ID:
NCT04583592
Group ID:
EG000
Title:
Camostat Mesilate
Description:
Participants will receive camostat mesilate for 14 days in addition to standard of care treatment.
Camostat Mesilate: Camostat mesilate administered as oral 100 mg round tablets. Study dose: Two 100 mg tablets (200 mg total) taken orally 4 times daily for 14 days.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
195
Other Number Affected:
8
Other Number At Risk:
195
Study:
NCT04583592
Results Section:
NCT04583592
Adverse Events Module:
NCT04583592