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 @ 3:30 AM
Ignite Modification Date:
2025-12-26 @ 2:12 AM
NCT ID:
NCT03243305
Group ID:
EG000
Title:
Interventional
Description:
This is a single-arm, open-label, Phase III study of AMPHORA, a non-hormonal contraceptive, at 112 sites in the United States (US) over seven cycles of use in women aged 18 to 35 years who are at risk of pregnancy.
AMPHORA: non-hormonal contraceptive vaginal gel
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
17
Serious Number At Risk:
1330
Other Number Affected:
601
Other Number At Risk:
1330
Study:
NCT03243305
Results Section:
NCT03243305
Adverse Events Module:
NCT03243305