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 @ 3:04 PM
Ignite Modification Date:
2025-12-25 @ 1:26 PM
NCT ID:
NCT04005859
Group ID:
EG000
Title:
CONTROL: IV Lido
Description:
CONTROL: Intravenous lidocaine, pre- and post-surgery (IV Lido)
IV Lidocaine: 1. Intravenous Lidocaine infusion (control arm, current standard of care) n= 35
1. 100 mg/5mL intravenous bolus of lidocaine 2% PF 5mL will be initiated by anesthesia service prior to general anesthesia induction.
2. 1.5 mg/kg/hr to begin prior to incision and continue until discontinued 1 hr postoperatively in PACU. Patients will be monitored in PACU for at least 30 minutes after discontinuation of lidocaine drip.
3. Adhesive tapes will be applied at the presumed level of TAP block puncture sites.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
28
Other Number Affected:
0
Other Number At Risk:
28
Study:
NCT04005859
Results Section:
NCT04005859
Adverse Events Module:
NCT04005859