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 @ 4:31 AM
Ignite Modification Date:
2025-12-26 @ 3:33 AM
NCT ID:
NCT02410018
Group ID:
EG000
Title:
Cohort 1 - Uterine Artery Embolization
Description:
Women treated with OCL 503 proceeding to hysterectomy 1 week post embolization.
OCL 503 will be administered by catheter to the uterine artery(ies) to achieve blood flow stasis.
OCL 503 (uterine artery embolization): Transcatheter embolization of the uterine artery(ies) using an embolic agent.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
2
Other Number Affected:
2
Other Number At Risk:
2
Study:
NCT02410018
Results Section:
NCT02410018
Adverse Events Module:
NCT02410018