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 @ 10:33 PM
Ignite Modification Date:
2025-12-25 @ 8:06 PM
NCT ID:
NCT06609135
Group ID:
EG000
Title:
Electrical Impedance Tomography (EIT) and CO2 Monitor
Description:
Participating infants will have the EIT belt placed at a minimum of twice per week throughout the NICU stay. A respiratory therapist or physician will place the EIT belt at the end of a feed and remove it at the next feed. A transcutaneous CO2 monitor will be placed concurrently.
Sentec LuMon Device (EIT system): Sentec EIT belts will be placed on infants up to once daily from consent through NICU discharge.
Sentec Digital Monitoring System (transcutaneous CO2 monitor): Sentec transcutaneous CO2 monitors will be placed on infants concurrently with EIT belts.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
20
Other Number Affected:
0
Other Number At Risk:
20
Study:
NCT06609135
Results Section:
NCT06609135
Adverse Events Module:
NCT06609135