Can cooled radiofrequency beat traditional heat for back pain?
NCT ID NCT07749599
First seen Aug 06, 2026 · Last updated Sep 04, 2026 · Updated 2 times
Summary
This trial compares two minimally invasive procedures—traditional bipolar radiofrequency and cooled radiofrequency—for treating chronic sacroiliac joint pain, a common cause of lower back pain. Adults aged 18-70 with persistent SI joint pain that hasn't improved with conservative care may participate. The study measures pain intensity and functional disability to see if one technique offers better or longer-lasting relief.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cooled radiofrequency and traditional bipolar radiofrequency procedures
- What this could lead to
- If successful, this could show that cooled radiofrequency provides longer-lasting pain relief and better function for people with sacroiliac joint pain, potentially becoming a preferred treatment option.
- What could go wrong
- This is a relatively small trial, and results may not apply to everyone. Both procedures carry risks like infection, bleeding, or nerve damage, and pain relief may not be permanent.
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
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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 70 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2029
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 to 70 years
- 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: * Age between 18-70 years * Chronic sacroiliac joint pain for ≥ 3 months * Pain intensity ≥ 5 on the Visual Analog Scale (VAS) * Positive SI joint provocative tests (at least 3 out of 5) * ≥ 50% pain relief following diagnostic SI joint block * Failure of conservative treatment for at least 6 weeks Exclusion Criteria: * Coagulopathy or anticoagulant therapy not appropriately managed * Local or systemic infection * Pregnancy * Severe psychiatric illness * Previous radiofrequency ablation of the SI joint * Spinal pathology explaining pain other than SI joint dysfunction
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Assuit university hospitals
Asyut, Egypt
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