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 @ 5:38 PM
Ignite Modification Date:
2025-12-25 @ 3:08 PM
NCT ID:
NCT01691768
Group ID:
EG001
Title:
Control
Description:
monthly 1% tenofovir gel provision and monitoring through CAPRISA research clinics
1% tenofovir gel: Participants will be randomized to receive 1% tenofovir gel through either:
* Public sector family planning services with 2-3 monthly provision and monitoring of 1% tenofovir gel and the use of QI methodology to promote reliable service delivery (intervention arm), or
* The CAPRISA research clinics with monthly provision and monitoring of 1% tenofovir gel (control arm).
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
17
Serious Number At Risk:
183
Other Number Affected:
181
Other Number At Risk:
183
Study:
NCT01691768
Results Section:
NCT01691768
Adverse Events Module:
NCT01691768