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 @ 4:26 AM
Ignite Modification Date:
2025-12-26 @ 3:30 AM
NCT ID:
NCT03468920
Group ID:
EG001
Title:
Arm 2: PO Acetaminophen Group
Description:
Patients randomized to Arm 2 will receive IV normal saline 100mL once and Acetaminophen 1000 mg PO once preoperatively
PO Acetaminophen: Acetaminophen PO 1000mg once pre-operatively
IV Solution Placebo: This will serve as the placebo for the IV Acetaminophen intervention
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
60
Other Number Affected:
0
Other Number At Risk:
60
Study:
NCT03468920
Results Section:
NCT03468920
Adverse Events Module:
NCT03468920