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 @ 2:44 AM
Ignite Modification Date:
2025-12-26 @ 1:24 AM
NCT ID:
NCT01330433
Group ID:
EG001
Title:
CoSeal Spray Group
Description:
CoSeal Spray will be applied at the end of the first staged procedure in patients randomized to the experimental group.
CoSeal Surgical Spray Group: A patient randomized to the CoSeal treatment group will have CoSeal Surgical Spray applied at the end of their first staged procedure.
The dose regimen is as follows:
* Patients weighing \< 3kg will receive 1ml of CoSeal
* Patients weighing 3-10kg will receive 1-2ml of CoSeal
* Patients weighing \>10kg will receive 2-4ml of CoSeal
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
19
Other Number Affected:
0
Other Number At Risk:
19
Study:
NCT01330433
Results Section:
NCT01330433
Adverse Events Module:
NCT01330433