Shocking pain away: higher voltage may ease chronic back pain
NCT ID NCT07303309
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a higher-voltage version of a nerve treatment (pulsed radiofrequency) could better relieve chronic pain in the lower back and leg. Twenty-two adults with pain lasting at least 12 weeks received either standard or high-voltage treatment. Researchers measured pain levels, disability, and safety over about six weeks.
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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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22 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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Apr 2025
- 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: * Adults aged ≥ 18 years old * Numeric Rating Scale (NRS-11) ≥ 4 at screening * Clinical diagnosis of lumbosacral radicular pain with symptom duration ≥ 12 weeks * Insufficient response to conservative therapy, including but not limited to pharmacotherapy and/or physiotherapy Exclusion Criteria: * Known hypersensitivity or allergy to medication required during the study (e.g., steroid, contrast media) * Coagulopathy, systemic infection, localized infection at needle-entry site, lumbar fracture, myelopathy, or severe organ dysfunction (e.g., renal failure, heart failure, severe respiratory diseases) * Comorbidities that compromise valid pain assessment (e.g., post-stroke, central neuropathy, malignancy) * Previous neurological deficits * Pregnancy * Refusal of participation in the study
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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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RSI Sultan Agung Islamic Teaching Hospital
Semarang, Central Java, 50112, Indonesia
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