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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03487120
Other study ID # NCTO
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 26, 2016
Est. completion date April 11, 2017

Study information

Verified date April 2023
Source Queen's University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A single blinded RCT for adult patients with spine pain. One group had a lumbar laminectomy with denervation of the facet joint at the level decompressed. The other group had a lumbar laminectomy without facet joint denervation. Both groups had their back pain and functional limitations measured using a 10 cm visual analogue scale and the Oswestry disability index (ODI). All measures were taken before surgery and at patients' 6, 12 and 24 week follow-up clinic visit.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date April 11, 2017
Est. primary completion date April 10, 2017
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - aged 19 or older - a diagnosis of spinal stenosis - having neurogenic claudication - complained of back pain for at least 3 months Exclusion Criteria: - previous surgery on their spine, - fracture, systemic inflammatory disease, - malignancies or an infection affecting their spine

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
facet joint denervation
Bipolar electrocautery

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Queen's University

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Visual analog scale for pain (VAS) 10 centimeter scale with a minimum of 0 indicating no pain and a maximum of 10 indicating worst pain. change from baseline score at 24 weeks
Secondary Change in Modified Oswestry Disability score (ODI) The ODI is divided into ten sections designed to assess limitations of various activities of daily living. Each section is scored on a 0-5 scale. The range of scores is 0 to a maximum of 60. The total score is multiplied by 2 and expressed as a percentage. A score of 0 to 20 points indicates minimal disability; 20 to 40 points, moderate disability; and 40 to 60 points, severe disability. change from baseline score at 24 weeks
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