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Comparison of Ultrasonic Osteotome and Conventional Drill Osteotome

Not Applicable
Completed
Conditions
Arthrodesis
Interventions
Device: drill
Device: ultrasonic osteotome
Registration Number
NCT02487901
Lead Sponsor
Seoul National University Hospital
Brief Summary

Ultrasonic bone osteotome has been utilized in various surgical field, but the use in neurosurgery especially in spine surgery is not widely spread. In the present study, the investigators are going to compare bony fusion rate after cervical laminotomy either with ultrasonic osteotome or conventional drill.

Detailed Description

Ultrasonic bone osteotome has been utilized in various surgical field, but the use in neurosurgery especially in spine surgery is not widely spread. The tissue selectivity of ultrasonic osteotomy may enhance operative time and reduce tissue trauma. Moreover, bony fusion rate may be increased because of low thermal injury to the bone. In the present study, we are going to compare bony fusion rate after cervical laminotomy either with ultrasonic osteotome or conventional drill.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
190
Inclusion Criteria
  1. cervical myelopathy at 3 or more levels due to spondylosis, congenital stenosis, or OPLL;
  2. aged more than 20 years
  3. with American Society of Anesthesiology physical status class 1 or 2
Exclusion Criteria
  1. concomitant neurological disease such as cerebral palsy or amyotrophic lateral sclerosis; 2) concurrent cancer or infection; 3) previous cervical spinal surgery; 4) a trauma-associated lesion; 5) inability to be followed up (i.e., foreign patients); 6) refusal to participate in the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Drilldrillmaking gutter on the hinge side of lamina with conventional drill
Ultrasonic osteotomeultrasonic osteotomemaking gutter on the hinge side of lamina with ultrasonic osteotome
Primary Outcome Measures
NameTimeMethod
Number of Participants With Bone Fusion6 months

Bone fusion based on computed tomography scan taken at postoperative 6 months

Secondary Outcome Measures
NameTimeMethod
Bleeding Amountduring operation

bleeding amount through suction and gauze, unit mL

Fracture of Laminarduring operation

The number of patients with lamina fractures.

Neck Pain/Arm Painpostop 1 year

Neck pain and arm pain were measured using a visual analogue scale (VAS), which is an integer with a minimum value of 0 and a maximum value of 10. Higher scores indicate a worse outcome.

Functional Outcomepostop 1 year

Functional outcomes were assessed using the Neck Disability Index (NDI).

The NDI consists of the following 10 subscales, each scored on a scale from 0 to 5:

Pain intensity (range: 0-5) Personal care (range: 0-5) Lifting (range: 0-5) Reading (range: 0-5) Headaches (range: 0-5) Concentration (range: 0-5) Work (range: 0-5) Driving (range: 0-5) Sleeping (range: 0-5) Recreation (range: 0-5) Each subscale has a minimum score of 0 and a maximum score of 5, with higher values indicating worse outcomes.

The total NDI score is calculated as the sum of all 10 subscale scores, ranging from 0 to 50. This total score is then converted into a percentage score (0-100%) by dividing the total score by 50 and multiplying by 100. Higher percentage scores indicate worse functional outcomes.

Trial Locations

Locations (1)

Seoul National University Hospital

🇰🇷

Seoul, Korea, Republic of

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