Pilot Study of Effect of Intravenous Lidocaine on Propofol Requirement in Facial Plastic Surgery

PHASE4CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

August 31, 2015

Primary Completion Date

May 31, 2016

Study Completion Date

May 31, 2016

Conditions
Anesthesia, Intravenous; Surgery, Plastic
Interventions
DRUG

lidocaine

Patients in lidocaine group will be received an intravenous bolus injection of 1.5 mg/kg lidocaine followed by a continuous infusion of 2 mg/kg/hr lidocaine.

DRUG

normal saline

Patients in control group will be received an intravenous bolus injection of 1.5 mg/kg normal saline followed by a continuous infusion of 2 mg/kg/hr normal saline.

DRUG

propofol

Propofol will be administered using target controlled infusion during monitored anesthesia care to adjust 60 to 80 of bispectral index.

Trial Locations (1)

156-755

Chung-Ang University Hospital, Seoul

All Listed Sponsors
lead

Chung-Ang University Hosptial, Chung-Ang University College of Medicine

OTHER

NCT02597140 - Pilot Study of Effect of Intravenous Lidocaine on Propofol Requirement in Facial Plastic Surgery | Biotech Hunter | Biotech Hunter