Cooled RFA vs Conventional RFA to Manage Chronic Facetogenic Low Back Pain

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

79 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-02-23

Study Completion Date

2023-07-31

Brief Summary

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This study is being conducted to assess the relative effectiveness of radiofrequency neurotomy in subjects with chronic axial low back pain originating in the lumbar facet joints using the COOLIEF\* Cooled Radiofrequency Probe as compared to the same procedure conducted using a Standard Radiofrequency Probe.

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Detailed Description

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This is a prospective, multi-center, randomized, single-blind comparison study examining the outcomes of subjects with chronic axial low back pain that originates in the lumbar facet joints undergoing a procedure to create a radiofrequency lesion in the medial branch nerves with either Cooled Radiofrequency Ablation (CRFA) or Conventional (Standard) Radiofrequency Ablation (SRFA). Approximately 188 participants from approximately 15 sites will be enrolled into this study, with subjects undergoing either CRFA or SRFA in a 1:1 randomization scheme. Follow-up will be conducted for 12 months post-treatment, with the primary endpoint being completed at month 6. Pain, overall outcome, quality of life, pain medication use, and adverse events will be compared between the two treatment groups to determine success.

Conditions

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Chronic Low-back Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

The study is a participant-blinded trial and deliberate action, utilizing a physical barrier, will be taken to ensure the blind remains intact.

Study Groups

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Cooled Radiofrequency

Cooled radiofrequency energy will be delivered to target medial branch nerves in the lower back to reduce pain

Group Type EXPERIMENTAL

Cooled Radiofrequency

Intervention Type DEVICE

Delivery of energy to ablate sensory nerves via cooled radiofrequency probe

Conventional Radiofrequency

Conventional radiofrequency energy will be delivered to target medial branch nerves in the lower back to reduce pain

Group Type ACTIVE_COMPARATOR

Conventional Radiofrequency

Intervention Type DEVICE

Delivery of energy to ablate sensory nerves via standard or conventional radiofrequency probe

Interventions

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Cooled Radiofrequency

Delivery of energy to ablate sensory nerves via cooled radiofrequency probe

Intervention Type DEVICE

Conventional Radiofrequency

Delivery of energy to ablate sensory nerves via standard or conventional radiofrequency probe

Intervention Type DEVICE

Other Intervention Names

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Coolief Standard Radiofrequency

Eligibility Criteria

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Inclusion Criteria

1. Age ≥ 21 years
2. Able to understand the informed consent form and provide written informed consent and able to complete outcome measures.
3. Subjects who have chronic axial (non-radicular) low back pain (at least 3 months) attributed to bilateral L4/L5, L5/S1 lumbar facet joint arthropathy based on clinical evaluation (paraspinal tenderness in the absence of signs and symptoms suggestive of focal neurological deficits) despite conservative treatments, including activity modification, home exercise, protective weight bearing, and/or analgesics (for example, acetaminophen or non-steroidal anti-inflammatory drugs \[NSAIDs\]).
4. Positive response to dual diagnostic medial branch blocks (defined as a decrease in numeric pain scores of at least 80% for a min of 3 hours for bupivacaine and minimum of 2 hours for lidocaine) using 0.5mL or less of 0.5% bupivacaine and 2% lidocaine, on respective encounters on separate days, at each of the appropriate medial branches.
5. Usual/Average Pain ≥ 6 on an 11-point NRS scale.
6. Analgesics including membrane stabilizers such as Neurontin (gabapentin) and antidepressants for pain, such as Cymbalta (duloxetine), must be clinically stable (defined as stable dosage for ≥ 6 weeks prior to the screening visit) and shall not change during the study without approval of the investigator.
7. Agree to see one physician (study physician) for back pain during the study period.
8. Subjects of child bearing potential must be willing to utilize double barrier contraceptive method for duration of participation.
9. Willingness to comply with the requirements of this protocol for the full duration of the study.

Exclusion Criteria

1. Evidence of inflammatory arthritis (example, rheumatoid arthritis) or other systemic condition (example; gout, fibromyalgia, MS, Lupus, etc.) that could cause pain.
2. Focal neurologic signs or symptoms.
3. Spinal pathology that may impede recovery such as spina bifida occulta, grade II or higher spondylolisthesis at an affected joint or adjacent level, or significant lumbar scoliosis (sagittal vertical axis angle \>5 degrees or Cobb Angle \>10 degrees).
4. Suspected mechanical instability based on flexion/extension and/or films at the proposed treatment levels
5. History of prior lumbar fusion or previous lumbar back surgery at the intended treatment levels.
6. Progressive motor deficit, and/or clinical signs of cauda equina or polyradiculopathy.
7. Radiologic evidence of a symptomatic herniated disc or nerve root impingement.
8. Symptomatic moderate or severe foramina or central canal stenosis demonstrating radicular symptoms or neurogenic claudication.
9. Evidence of neuropathic pain affecting the lower back.
10. Intra-articular steroid injection at target levels within 90 days from randomization.
11. Platelet rich plasma (PRP) or stem cells at target levels within 180 days from randomization.
12. Prior lumbar radiofrequency neurotomy of the L3/L4, L4/L5 medial branches and/or L5/S1dorsal ramus.
13. Body mass index (BMI) \> 40 kg/m2
14. Extremely thin patients and those with minimal subcutaneous tissue thickness that would not accommodate a radiofrequency lesion of up to 14 mm in diameter to limit the risk of skin burns.
15. Active joint infection or systemic or localized infection at needle entry sites (subject may be considered for inclusion once infection is resolved).
16. Pending or active compensation claim, litigation, or disability remuneration (e.g. disability, worker's compensation, auto injury in litigation or pending litigation).
17. Pregnant, nursing or intent of becoming pregnant during the study period
18. Chronic pain associated with significant psychosocial dysfunction.
19. Poorly controlled severe psychiatric illness or ongoing psychological barriers to recovery, as determined by the investigator.
20. Allergies to any of the medications to be used during the procedures
21. History of uncontrolled coagulopathy, ongoing coagulation treatment that cannot be safely interrupted for procedure, or unexplained or uncontrollable bleeding that is uncorrectable.
22. Identifiable anatomical variability that would materially alter the procedure as described in the protocol.
23. Within the preceding 2 years, subject has suffered from active narcotic addiction, substance, or alcohol abuse.
24. Current prescribed opioid medications greater than 50 morphine equivalent daily opioid dose.
25. Uncontrolled immunosuppression (e.g. AIDS, cancer, diabetes, etc.).
26. Subject currently implanted with pacemaker, stimulator or defibrillator.
27. Participating in another clinical trial/investigation which included therapeutic treatment within 30 days prior to signing informed consent.
28. Subject unwilling or unable to comply with follow up schedule, protocol requirements or procedures.

Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No