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Ultrasound Measured Epidural Depth for Midline Approach in Pediatric Patients With Scoliosis: Prospective Observational Study

Yonsei University logo

Yonsei University

Status

Unknown

Conditions

Scoliosis

Treatments

Device: Ultrasound

Study type

Observational

Funder types

Other

Identifiers

NCT04877964
4-2021-0266

Details and patient eligibility

About

The purpose of this study was to

  1. investigate the degree of agreement between the ultrasound-measured depth (in the transverse median and paramedian sagittal oblique plane) and the actual depth to the epidural space in pediatric patients with scoliosis.
  2. investigate the quality of ultrasound view for detecting ligamentum flavum and dura mater.

Enrollment

55 estimated patients

Sex

All

Ages

3 to 14 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. pediatric patients (aged 3-14 years) with scoliosis (cobb angle >10 degree) scheduled for correctional osteotomy of the lower extremity and requesting epidural analgesia for postoperative pain control

Exclusion criteria

  1. Contraindications to epidural analgesia (local infection, blood clotting disorder, anatomical abnormality, sepsis, etc.)
  2. If all of the parents of the subject are foreigners or illiterate (if the parents of the subject can not read the agreement)

Trial design

55 participants in 1 patient group

pediatric patients with scoliosis
Description:
Patients aged 3-14 years with scoliosis and who request epidural analgesia
Treatment:
Device: Ultrasound

Trial contacts and locations

1

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Central trial contact

Hye Jin Kim, MD

Data sourced from clinicaltrials.gov

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