The Effect of Intraoperative Intravenous Lidocaine Infusion on Postoperative Pain and Recovery in Children (< 7 Years Old) Undergoing Thoracoscopic Surgery:Prospective, Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This study aims to investigate the efficacy of intraoperative intravenous lidocaine infusion on postoperative pain management and recovery in pediatric patients undergoing thoracoscopic pulmonary resection.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6 months
Maximum Age: 7
Healthy Volunteers: f
View:

• Pediatric patients aged under 7 years undergoing thoracoscopic pulmonary resection

Locations
Other Locations
Republic of Korea
Seoul National University Hospital
RECRUITING
Seoul
Contact Information
Primary
Ji-Hyun Lee, MD, PhD
muslab6@snu.ac.kr
82-2-2072-3661
Time Frame
Start Date: 2024-12-09
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 80
Treatments
Experimental: Lidocaine group
Anesthesia induction is performed according to the standard protocol. Monitoring includes electrocardiography, pulse oximetry, arterial blood pressure, depth of anesthesia (Patient State Index, PSI), and pain score (Analgesia Nociception Index).~In the lidocaine group, a single bolus dose of lidocaine 1.5 mg/kg is administered concurrently with the induction of anesthesia, followed by a continuous infusion of lidocaine at a rate of 1.5 mg/kg/hr.
Placebo_comparator: Control group
The control group receives a continuous infusion of normal saline in the same volume as that administered to the lidocaine group.
Related Therapeutic Areas
Sponsors
Leads: Seoul National University Hospital

This content was sourced from clinicaltrials.gov

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