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 @ 4:51 PM
Ignite Modification Date:
2025-12-25 @ 2:35 PM
NCT ID:
NCT02988050
Group ID:
EG000
Title:
Propofol-dexmedetomidine
Description:
Propofol-dexmedetomidine Bupivacaine; Lidocaine (local anaesthetics) Epinephrine (with local anaesthetics for skin infiltration)
Dexmedetomidine: Dexmedetomidine used for conscious sedation.
Propofol: Used for conscious sedation.
Bupivacaine: Local anaesthetics
Lidocaine: Local anaesthetic
Epinephrine: With local anaesthetic for skin infiltration.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
30
Other Number Affected:
0
Other Number At Risk:
30
Study:
NCT02988050
Results Section:
NCT02988050
Adverse Events Module:
NCT02988050