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

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Yonsei University

Status

Completed

Conditions

Inguinal Hernia

Treatments

Drug: Normal saline infusion
Drug: Systemic intravenous lidocaine infusion

Study type

Interventional

Funder types

Other

Identifiers

NCT02007330
4-2013-0692

Details and patient eligibility

About

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

Enrollment

66 patients

Sex

All

Ages

1 to 6 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

66 participants in 2 patient groups, including a placebo group

Group L
Experimental group
Description:
Intravenous lidocaine infusion group
Treatment:
Drug: Systemic intravenous lidocaine infusion
Group C
Placebo Comparator group
Description:
Intravenous normal saline infusion - control group
Treatment:
Drug: Normal saline infusion

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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