Freeze or burn? new study tests two nerve treatments for back pain
NCT ID NCT06804551
First seen Jun 27, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This study compares two treatments for chronic low back pain caused by facet joints: standard radiofrequency ablation (RFA), which burns pain nerves, and a newer freezing method called iovera°. Both aim to block pain signals temporarily. About 30 adults with long-term back pain will receive one of the treatments and report their pain levels over a year. The goal is to see if freezing is as effective as burning, with possibly fewer side effects.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2025
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Subjects must meet all the following inclusion criteria to be eligible for participation. * Subjects at least 18 years of age at Screening * Chronic low back pain (≥ 3 months) * Successful trial of two diagnostic medial branch blocks * Failure of at least three months of conservative non-operative therapy (e.g., physical therapy, chiropractic care, sleep hygiene, weight loss, spinal injections, NSAIDs, physician-directed exercise program or other appropriate pain medicine) * Able to provide informed consent, adhere to the study visit schedule, and complete all study assessments Exclusion Criteria: Subjects who meet any of the following exclusion criteria will not be eligible for participation in this study. * Active workers' compensation, personal injury, Social Security disability insurance (SSDI), or other litigation/compensation related to the spine * Infection in the back or open wounds in the back * Cancer * Fractures in the back * Pain shooting down the leg * Pain when walking up/downhill * Any back surgery or metal objects in the back * Any implants of any kind in the body * Currently pregnant, nursing, or planning to become pregnant during the study * Blood clots * History of RFA treatment in back * Drug abuse
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Kansas Medical Center
Kansas City, Kansas, 66160, United States
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