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:
2025-12-26 @ 11:48 AM
Ignite Modification Date:
2025-12-26 @ 11:48 AM
NCT ID:
NCT03052816
Group ID:
EG001
Title:
Standard
Description:
1. Motrin 600mg PO Q4h PRN pain 1-3
2. Percocet 1 tab PO Q4-6 hours PRN 4-6 pain
3. Percocet 2 tabs PO Q 7-10 hours PRN 7-10 pain
4. Patients will receive dilaudid 0.2mg IV Q3 hr PRN for breakthrough pain.
5. Patients will be discharged home with Motrin and Percocet for pain PRN.
Motrin/Percocet/Dilaudid for breakthrough: Standard regimen
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
33
Other Number Affected:
0
Other Number At Risk:
33
Study:
NCT03052816
Results Section:
NCT03052816
Adverse Events Module:
NCT03052816