New cannula design may improve back pain procedure outcomes
NCT ID NCT07475689
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested two different cannula designs used during radiofrequency ablation for chronic low back pain caused by facet joints. 82 adults were randomly assigned to receive the procedure with either a standard straight cannula or a sidekick cannula. Researchers measured pain reduction and functional improvement to see if one design works better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- radiofrequency ablation procedure
- What this could lead to
- If one cannula design proves better, it could improve pain relief and function for people with chronic low back pain from facet joints.
- What could go wrong
- This is a small, single-center study with 82 participants. Results may not apply to everyone, and the procedure itself carries risks like infection or nerve damage.
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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82 people
The number who actually took part.
- Started
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Aug 2024
- Finished
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Sep 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.
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 ≥18 years * Chronic lumbar facet-mediated low back pain lasting more than 3 months * Failure of conservative treatment including physical therapy and medical management * Positive diagnostic medial branch block * Patients scheduled for lumbar medial branch radiofrequency ablation Exclusion Criteria: * Previous lumbar radiofrequency ablation at the same level * Coagulopathy or anticoagulant therapy that cannot be discontinued * Local infection at the procedure site * Severe spinal deformity or instability * Pregnancy * Inability to provide informed consent
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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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Gulhane Training and Research Hospital, Department of Anesthesiology and Reanimation
Ankara, 06010, Turkey (Türkiye)