Medial Branch Radiofrequency Ablation and Lumbar Multifidi

Osteoarthritis Clinical Trial

Official title:

The Effect of Medial Branch Radiofrequency Ablation on Functional Spinal Stability and Lumbar Multifidi Muscle Architecture Assessed by Magnetic Resonance Imaging and Ultrasound Imaging

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03744260
• Other study ID #: AAAR1440
• Status: Completed
• Start date: January 1, 2017
• Est. completion date: June 30, 2020

Study information

• Verified date: July 2020
• Source: Columbia University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of this study is to evaluate the effects of lumbar medial branch radiofrequency ablation (RFA) on lumbar multifidi muscle size and clinical spinal stability. Specifically, this study is designed to highlight the comparison of multifidi muscle architecture using ultrasound imaging (USI) and MRI before and after lumbar medial branch RFA. This study will also include a commonly utilized functional assessment of the lumbar spine to evaluate the effects of RFA on lumbar spinal stability.

Description:

Radiofrequency ablation (RFA) for the lumbar spine (lower back) is a procedure used to treat lower back pain secondary to facet arthritis. The procedure ablates (burns) a small nerve that goes to the arthritic joint in the back. This nerve also innervates a muscle called the multifidus, thought to be important for lumbar stability. The investigators are conducting a study to evaluate if RFA has any impact on multifidi size, spinal stability, and overall function. The tools the investigators will be using to assess the multifidi muscles are musculoskeletal ultrasound, MRI, physical therapy assessment, and functional questionnaires. The goal of the study is to determine if RFA impacts the multifidi in a clinically significant fashion, causing atrophy, spinal instability, and/or functional decline.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 4
• Est. completion date: June 30, 2020
• Est. primary completion date: June 30, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion criteria are:

• Aged over 18 years

• Presence of lumbar spondylosis or facet arthropathy (as determined by a radiologist) *Unilateral back pain without radicular symptoms

• Positive physical findings for facet mediated pain (pain with lumbar extension and rotation to affected side)

• Ability to complete outcome measure forms.

Exclusion criteria are:

• Prior spinal surgery

• Prior RFA procedures

• Pregnancy

• Contraindications to MRI

• Presence of therapeutic anti-coagulation, medical co-morbidities that would interfere with the ability to perform the procedure safely

• Presence of neurologic changes

• Active tobacco smoking history

• Presence of active litigation

• Presence of open workers compensation case

Related Conditions & MeSH terms

• Osteoarthritis
• Spondylosis

Intervention

Diagnostic Test:
• Patients undergo ultrasound and lumbar MRI
Patients undergo ultrasound, physical therapy exam and MRI before and after the radiofrequency ablation procedure that they are getting as part of their regular care.

Locations

Country	Name	City	State
United States	Columbia University Vagelos College of Physicians and Surgeons	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
Columbia University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage Change in Volume of multifidus muscle on MRI	Analysis will include volumetric measurements of the multifidi as well as volumetric assessments of the muscle with fat subtracted.	Up to 3 months after radiofrequency ablation procedure
Primary	Percentage Change in Cross Sectional Area of Multifidi	Area will be measured by MRI scan.	Up to 3 months after radiofrequency ablation procedure
Secondary	Score on Numeric Pain Rating Scale (NPRS)	The Numeric Pain Rating Scale (NPRS) is a unidimensional measure of pain intensity in adults. Respondents are asked to select a whole number (0-10 integers) that best reflects the intensity of his/her pain. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable").	Up to 3 months after radiofrequency ablation procedure
Secondary	Percentage Score on the Modified Oswestry Disability Index	This is a patient-completed questionnaire which gives a subjective percentage score of level of function (disability) in activities of daily living in those rehabilitating from low back pain. It examines perceived level of disability in 10 everyday activities of daily living, which each statement scored from 0 (no disability) to 5 (worst pain). An aggregate score (percentage) is then calculated, with 0% indicating no disability to 100%, indicating crippled or bed-bound.	Up to 3 months after radiofrequency ablation procedure