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The Effect of Systemic Lidocaine Infusion to Postoperative Pain and Quality of Recovery After Laparoscopic Hernia Repair in Children

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02007330
Enrollment
66
Registered
2013-12-10
Start date
2013-11-30
Completion date
2015-01-31
Last updated
2015-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inguinal Hernia

Keywords

systemic lidocaine, postoperative pain, recovery, pediatric, inguinal hernia, laparoscopy

Brief summary

Systemic lidocaine administration may improve postoperative pain and recovery after laparoscopic inguinal hernia repair in pediatric patients

Interventions

In group L, intravenous lidocaine infusion (0.1mg/kg) for 1minutes after induction of anesthesia. After 1 minutes, lidocaine infusion continued at rate of 1.5mg/kg/hr during operation, and discontinued before move the patients to PACU.

In group C, the patients receive same volume of normal saline

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
1 Years to 6 Years
Healthy volunteers
No

Inclusion criteria

* Age between 1 and 6 year-old * ASA class 1 and 2 * Pediatric Inguinal hernia patients who are scheduled for elective laparoscopic inguinal hernia repair

Exclusion criteria

* Allergy to local anesthetics or contraindication to use of lidocaine * Current active upper respiratory infection or history of upper respiratory infection within 2 weeks * Severe cardiovascular disease * Renal failure * Liver failure * Neurologic and psychologic disease * Chronic treatment with analgesics * Previous history of laparoscopic operation * Parents' refusal

Design outcomes

Primary

MeasureTime frameDescription
Assessing postoperative pain24 hours after operationAssessing FLACC(Face-Legs-Activity-Crying-Consolability) score at 4, 8, 12 and 24hours after operation

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026