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 @ 4:12 PM
Ignite Modification Date:
2025-12-25 @ 2:12 PM
NCT ID:
NCT06225466
Group ID:
EG001
Title:
No Neuromuscular Blockade
Description:
Anesthesia will be administered in a standard fashion. Rocuronium and sugammadex will not be administered.
SOC drugs:
1. Midazolam 0.5 mg/kg (max 15 mg) and acetaminophen 15 mg/kg (max 800 mg) PO 20-30 minutes before surgery.
2. Sevoflurane induction and maintenance of anesthesia
3. Dexamethasone 0.5 mg/kg IV (max 8 mg) intraop
4. Dexmedetomidine 0.3 mcg/kg IV (max 12 mcg) intraop
5. Fentanyl at the discretion of the anesthesiologist. In the post-anesthesia care unit (PACU), fentanyl 0.5 mcg/kg IV (max 25 mcg) for pain score 4 or greater (max 3 doses).
6. Ondansetron 0.1 mg/kg (max 4 mg) IV intraop
7. Ibuprofen 10 mg/kg (max 500 mg) PO every 6 hours beginning after surgery and alternating with acetaminophen 15 mg/kg (max 800 mg) every 6 hours.
Device monitoring:
1. Bispectral index system intraop
2. ExSpiron respiratory volume monitor intraop and in PACU
Anesthesia without neuromuscular blockade: Anesthesia without rocuronium or sugammadex
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
86
Other Number Affected:
1
Other Number At Risk:
86
Study:
NCT06225466
Results Section:
NCT06225466
Adverse Events Module:
NCT06225466