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 @ 10:16 PM
Ignite Modification Date:
2025-12-25 @ 7:50 PM
NCT ID:
NCT00638235
Group ID:
EG007
Title:
Phase VI (Elevate Anterior Gen 1, EU Only)
Description:
AMS Elevate™ Anterior \& Apical with IntePro Lite: Mesh for the treatment of anterior \& apical vaginal wall prolapse (Generation 1, For PROPEL Study Use Only) Phase VI ended after 12M visit because next generation of Elevate Anterior was already under trial in Phase VII
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
35
Other Number Affected:
7
Other Number At Risk:
35
Study:
NCT00638235
Results Section:
NCT00638235
Adverse Events Module:
NCT00638235