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 @ 9:23 PM
Ignite Modification Date:
2025-12-25 @ 7:09 PM
NCT ID:
NCT05342532
Group ID:
EG000
Title:
High Dose Dual Therapy
Description:
This regimen includes a 14-day course of amoxicillin 1 g three times daily and omeprazole 40 mg three times daily.
Amoxicillin: 1 g
Omeprazole: 40 mg. Patients were asked to take omeprazole one hour prior to food intake, while antibiotics were taken after meals.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
58
Other Number Affected:
5
Other Number At Risk:
58
Study:
NCT05342532
Results Section:
NCT05342532
Adverse Events Module:
NCT05342532