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 @ 4:27 AM
Ignite Modification Date:
2025-12-26 @ 3:31 AM
NCT ID:
NCT04547920
Group ID:
EG000
Title:
12 Weeks Followed by Optional 12 Month Continuation
Description:
Initial 12 Weeks: Patients were instructed to complete therapy with a wearable closed-loop, continuous sensing tibial nerve stimulation device for bladder modulation.
Optional Months 4-12: Subjects who qualified for the long-term follow up and elected to enroll, signed a new informed consent and continued therapy for the duration of the study.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
96
Other Number Affected:
17
Other Number At Risk:
96
Study:
NCT04547920
Results Section:
NCT04547920
Adverse Events Module:
NCT04547920