Clinical Trials Directory

Trials / Completed

CompletedNCT03459105

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
44 (actual)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREUltrasound-assisted paramedian spinal anesthesiaA preprocedural ultrasound scanning will be done, and skin marking will be made. The needle entry point and insertion angle will be determined based on ultrasound scanning. Spinal anesthesia will be performed via paramedian approach.
PROCEDURELandmark-guided spinal anesthesiaSpinal anesthesia will be done using conventional landmark-guided technique.
DRUG0.5% heavy bupivacaine0.5% heavy bupivacaine will be administered into intrathecal space. The dose of local anesthetic injected for spinal anesthesia will be at the discretion of the attending anesthesiologist. The dose range of intrathecal bupivacaine will be between 12 and 16 mg.

Timeline

Start date
2018-03-13
Primary completion
2018-07-04
Completion
2018-07-05
First posted
2018-03-08
Last updated
2019-01-03

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03459105. Inclusion in this directory is not an endorsement.