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 @ 7:58 PM
Ignite Modification Date:
2025-12-25 @ 5:32 PM
NCT ID:
NCT03738904
Group ID:
EG000
Title:
Arm 1 (Multimodal ERAS)
Description:
Arm1 (Multimodal ERAS):
Preoperative:
oral gabapentin 600mg and oral acetaminophen 1,000mg
Postoperative pain control:
1. Gabapentin oral 300 mg TID (#42, refill #1)
2. Acetaminophen oral 1000mg TID (#42, refill #1)
3. Ketorolac oral 10 mg TID (#15, refill #0)
4. Oxycodone oral 5 mg PRN every 6 hours (#30, refill #0)
Postoperative laxative regimen:
1. Daily MiraLAX 1 scoop in 1 glass of water for 15 days
2. Daily milk of magnesia 1 tablespoon if no bowel movement by POD2 until regular bowel movements
3. Daily mineral oil 1 table spoon if no bowel movement by POD2 until regular bowel movements
ERAS: Gabapentin Acetaminophen Ketoroloac IV (intraop) and PO Dexamethasone (included with benzocaine in local anesthesia) Oxycodone PO Polyethylene glycol
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
45
Other Number Affected:
4
Other Number At Risk:
45
Study:
NCT03738904
Results Section:
NCT03738904
Adverse Events Module:
NCT03738904