ClinicalTrials.Veeva

Menu

Ultrasonographic Evaluation of Drug Spread in Epidural Space During Caudal Block in Children

Yonsei University logo

Yonsei University

Status

Completed

Conditions

Children Who Need Urological Surgery

Study type

Observational

Funder types

Other

Identifiers

NCT01340313
4-2010-0775

Details and patient eligibility

About

Caudal block is the world-widely used technique for an effective postoperative analgesia in children undergoing OPD-based infra-umbilical surgery. Because the caudal block is usually performed with a single-shot, proper dosage is required to achieve sufficient analgesic levels. Several clinical researches have been performed to assess the drug spread levels using mathematical equation, X-ray evaluation, and ultrasonography during caudal block in children. In our previous study using fluoroscopy, we obtained the results that the established weight-based doses provided adequate block levels for each type of surgery.

Ultrasonography is precise tool to evaluate the spinal structures and can provide estimated information in real time during caudal or epidural block in children.

The aim of this study is to evaluate the drug spread level with a weight-based doses using ultrasonography during caudal block in children and assess the reliability of the real time ultrasonography to determine the drug spread levels. After general anesthesia, the patient will be placed in lateral decubitus position for caudal block. Total 1.5 ml/kg of 0.15% ropivacaine will be injected into the caudal space. The spread level will be step-wise evaluated using ultrasonography at the injected drug dose of 0.5 ml/kg, 1.0 ml/kg, 1.25 ml/kg, and 1.5 ml/kg.

Enrollment

72 patients

Sex

All

Ages

3 months to 5 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • children who needed caudal block for postoperative analgesia (age 3 months ~ 5 years old)
  • Consent from one of parents 3. ASA physical status I or II

Exclusion criteria

  • bleeding tendency
  • spinal anomaly
  • infection focus on back
  • allergic reaction to local anesthetics
  • foreigner of illiteracy who cannot read consent form

Trial design

72 participants in 1 patient group

Group 1
Description:
4 times evaluation according to doses in 1 group

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems