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Recruiting Phase 4 NCT06710405

NCT06710405 The Effect of Intraoperative Intravenous Lidocaine Infusion on Postoperative Pain and Recovery in Children (< 7 Years Old) Undergoing Thoracoscopic Surgery

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Clinical Trial Summary
NCT ID NCT06710405
Status Recruiting
Phase Phase 4
Sponsor Seoul National University Hospital
Condition Pain Management After Surgery
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2024-12-09
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 6 Months
Max Age 7 Years
Study Type INTERVENTIONAL
Interventions
Lidocaine (drug)Saline infusion (placebo)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 4 studies follow an already-approved treatment in real-world conditions to monitor long-term safety and effectiveness.

This trial targets 80 participants in total. It began in 2024-12-09 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 Criteria

Inclusion Criteria: * Pediatric patients aged under 7 years undergoing thoracoscopic pulmonary resection Exclusion Criteria: * cardiac dysfunction requiring vasopressors or inotropic agents * atrioventricular block or bradycardia * Liver or kidney dysfunction * Hypersensitivity to local anesthetics

Contact & Investigator

Central Contact

Ji-Hyun Lee, MD, PhD

✉ muslab6@snu.ac.kr

📞 82-2-2072-3661

Frequently Asked Questions

Who can join the NCT06710405 clinical trial?

This trial is open to participants of all sexes, aged 6 Months or older, up to 7 Years, studying Pain Management After Surgery. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06710405 trial and what does that mean for participants?

Phase 4 studies are conducted after a treatment has been approved. They monitor long-term safety and real-world effectiveness in a broader patient population.

Is NCT06710405 currently recruiting?

Yes, NCT06710405 is actively recruiting participants. Contact the research team at muslab6@snu.ac.kr for enrollment information.

Where is the NCT06710405 trial being conducted?

This trial is being conducted at Seoul, South Korea.

Who is sponsoring the NCT06710405 clinical trial?

NCT06710405 is sponsored by Seoul National University Hospital. The trial plans to enroll 80 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology