RFA Using Multi-Tined Electrodes vs.Traditional Electrodes for Lumbar Spondylosis

NCT ID
NCT06477094
Registry status
Recruiting
Study type
Not specified in the registry data
Phase
Not applicable
Sponsor
University of Arkansas

Overview

ClinicalTrials.gov lists this study as Recruiting.

Enrollment: 25 participants (Estimated).

What is being studied

No interventions are listed in the registry data.

Who may be eligible

Ages
Not specified in the registry data
Sex
Not specified in the registry data
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: 1. Greater than 18 years of age 2. Presenting with chronic non-radicular lower back pain 3. Failure of conservative treatment such as physical therapy or NSAID usage 4. Diagnosis of lumbar facet mediated lower back pain by a board-certified chronic pain physician via two sets of prognostic lumbar MBBs with 0.5cc of 0.5% bupivacaine with \>80% pain relief Exclusion Criteria: 1. History of known coagulopathy 2. \> 3 American Society of Anesthesiologists Classification 3. Pregnancy 4. Spinal hardware between L3 and S1 5. Allergies to injection medications 6. English illiteracy 7. Pain improvement following physical therapy or NSAID usage 8. Previous history of attempted lumbar RFA

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: United States

  • Arkansas, United States: 1

Sample of listed locations

  • University of Arkansas for Medical Sciences — Little Rock, Arkansas, 72205, United States — Site recruitment status not specified in the registry data

Study details

Start date
August 9, 2024
Primary completion date
July 31, 2027
First posted
June 27, 2024

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT06477094
Registry last updated
September 10, 2026
QualifiedStudies registry data refreshed
September 21, 2026

View NCT06477094 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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