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 @ 4:05 AM
Ignite Modification Date:
2025-12-26 @ 3:01 AM
NCT ID:
NCT01463202
Group ID:
EG001
Title:
DMPA at 4-6 Weeks After Delivery
Description:
Depot medroxyprogesterone acetate at 4-6 weeks after delivery
Depot medroxyprogesterone acetate: Delayed administration of DMPA (4-6 weeks postpartum)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
78
Other Number Affected:
0
Other Number At Risk:
78
Study:
NCT01463202
Results Section:
NCT01463202
Adverse Events Module:
NCT01463202