Can a gentle electric pulse ease chronic nerve pain?
NCT ID NCT01117870
First seen Aug 28, 2026 ยท Last updated Aug 28, 2026
Summary
This trial tests whether pulsed radiofrequency, a technique that applies short bursts of electrical energy to a nerve, can reduce chronic lumbar radicular pain, a type of back and leg pain. Adults with pain lasting at least 4 months and matching MRI or CT findings receive either the real treatment or a placebo needle. The study measures pain changes and whether a larger trial is feasible.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pulsed radiofrequency applied to the dorsal root ganglion
- What this could lead to
- If it works, this could offer a non-damaging, needle-based option for people with chronic leg and back pain, and support a larger study.
- What could go wrong
- This is a small, early trial with only 31 participants, so results may not apply widely. The treatment may not outperform placebo, and there are standard risks like bleeding or infection.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
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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31 people
The number who actually took part.
- Start date
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Jul 2010
- Finished
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Nov 2012
- 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
-
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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * \> 18 years of age * CLR for at least 4 months of more, with concordant findings on either MRI and CT scan * VAS score of at least 60/100 at presentation * informed consent Exclusion Criteria: * \< 18 years of age * patient refusal * any contraindication to neuraxial injection such as coagulation disturbance, anticoagulant therapy, bleeding disorder, or infection at site of injection * anatomical deformity or derangement, either congenital or surgical such as: extreme scoliosis, previous implant or instrumentation making it difficult to access the foramen as evidence by MRI, CT, or plain x-rays * uncontrolled diabetes or severe coronary vascular disease necessitating continuation of anticoagulation therapy * known history of psychiatric illness-such as depression or psychosis * presence of cancer accounting for present symptoms * patient's inability of communicate in English and inability to understand and fill out the required follow-up questionnaire and form * allergy to local anesthetics or steroid or contrast medium * any patient with a history of acute neurological weakness or neurodeficit in the affected limb in terms of measurable motor weakness or abnormal reflexes
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Conditions
The condition(s) this trial relates to.
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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East End Clinic, St. Joseph's Healthcare Hamilton
Hamilton, Ontario, L8N 4A6, Canada
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