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Midline vs. Paramedian Approaches for US-assisted Spinal Anesthesia

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Seoul National University

Status

Completed

Conditions

Ultrasonography
Anesthesia, Spinal

Treatments

Procedure: ultrasound-assisted paramedian approach
Procedure: ultrasound-assisted midline approach

Study type

Interventional

Funder types

Other

Identifiers

NCT03491943
H-1803-060-928

Details and patient eligibility

About

Ultrasound has emerged as an useful tool for neuraxial blockade. The aim of this study is to compare the efficacy and safety between the midline approach and paramedian approach for ultrasound-assisted spinal anesthesia in adult patients.

Enrollment

112 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients scheduled to undergoing elective orthopedic surgery under spinal anesthesia, with ASA physical status classification I, II, III

Exclusion criteria

  • Patients with contraindication to spinal anesthesia (coagulopathy, local infection, allergy to local anesthetic)
  • Patients with morbid cardiac diseases
  • Pregnancy
  • Patients with previous history of lumbar spinal surgery
  • Patients with anatomical abnormality of lumbar spine

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

112 participants in 2 patient groups

Midline group
Experimental group
Description:
Preprocedural ultrasound-assisted midline approach of spinal anesthesia will be performed. 0.5% heavy bupivacaine will be injected to intrathecal space for spinal anesthesia.
Treatment:
Procedure: ultrasound-assisted midline approach
Paramedian group
Active Comparator group
Description:
Preprocedural ultrasound-assisted paramedian approach of spinal anesthesia will be performed. 0.5% heavy bupivacaine will be injected to intrathecal space for spinal anesthesia.
Treatment:
Procedure: ultrasound-assisted paramedian approach

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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