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ENROLLING BY INVITATION
NCT07193836
NA

Synergistic Effect of Intravenous Lidocaine on Anesthetic Induction and Emergence in Patients Undergoing Laparoscopic Cholecystectomy or Gynecological Surgery

Sponsor: General Hospital of Ningxia Medical University

View on ClinicalTrials.gov

Summary

This study aims to evaluate the effect of intravenous lidocaine on consciousness changes during anesthesia in patients undergoing laparoscopic cholecystectomy or gynecologic surgery. A total of 150 patients will be randomly assigned to one of three groups: a single-dose lidocaine group, a continuous-infusion group, or a placebo group. All patients will receive standard anesthesia care, and the study will monitor brain activity using EEG-based PSi values to measure anesthesia induction time, recovery time, and changes in consciousness. The goal is to determine whether lidocaine can reduce the amount of anesthetic used, shorten the time to fall asleep, and promote faster awakening after surgery. The results may help improve anesthesia safety and enhance recovery in surgical patients.

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

195

Start Date

2025-09-25

Completion Date

2025-12-31

Last Updated

2025-09-26

Healthy Volunteers

No

Interventions

DRUG

Normal Saline (0.9% NaCl)

Participants in the control group received a single intravenous injection of 0.9% normal saline at induction of anesthesia.

DRUG

Lidocaine

Participants in this group received a single intravenous bolus of lidocaine (1.5 mg/kg) at anesthesia induction. No additional lidocaine was administered thereafter.

DRUG

Lidocaine Bolus + Infusion

Participants in this group received a bolus of lidocaine (1.5 mg/kg) at induction followed by continuous intravenous infusion of lidocaine (2 mg/kg/h) until the end of surgery.

Locations (1)

General Hospital of Ningxia Medical University

Yinchuan, Ningxia, China