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Ultrasound-assisted Versus Conventional Landmark-guided Spinal Anesthesia in Patients With Abnormal Spinal Anatomy

Seoul National University logo

Seoul National University

Status

Completed

Conditions

Ultrasonography
Anesthesia, Spinal
Scoliosis

Treatments

Drug: 0.5% heavy bupivacaine
Procedure: Ultrasound-assisted paramedian spinal anesthesia
Procedure: Landmark-guided spinal anesthesia

Study type

Interventional

Funder types

Other

Identifiers

NCT03459105
1801-107-917

Details and patient eligibility

About

Spinal anesthesia can be challenging in patients with lumbar scoliosis or previous lumbar spine surgery. This study aims to evaluate whether the use of the ultrasound-assisted spinal anesthesia reduces the number of passes required to successful dural puncture compared with the conventional surface landmark-guided technique in patients with abnormal spinal anatomy.

Enrollment

44 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,

  • and with (1) or (2)

    1. documented scoliosis in preoperative L-S-Spine X-ray (Cobb abgle > 10 degree)
    2. previous history of lumbar spinal surgery

Exclusion criteria

  • Patients with contraindication to spinal anesthesia (coagulopathy, local infection, allergy to local anesthetic)
  • Patients with morbid cardiac diseases
  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

44 participants in 2 patient groups

Ultrasound-assisted
Experimental group
Description:
Preprocedural ultrasound-assisted paramedian spinal anesthesia will be performed. 0.5% heavy bupivacaine will be injected to intrathecal space for spinal anesthesia.
Treatment:
Procedure: Ultrasound-assisted paramedian spinal anesthesia
Drug: 0.5% heavy bupivacaine
Landmark-guided
Active Comparator group
Description:
Landmark-guided spinal anesthesia will be performed, via either midline or paramedian approach. 0.5% heavy bupivacaine will be injected to intrathecal space for spinal anesthesia.
Treatment:
Procedure: Landmark-guided spinal anesthesia
Drug: 0.5% heavy bupivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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