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New cannula design may improve back pain procedure outcomes

NCT ID NCT07475689

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

82 people

The number who actually took part.

Started

Aug 2024

Finished

Sep 2025

Lead sponsor

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

Anyone

Healthy volunteers

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

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.

Back Pain Low Back Pain

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Gulhane Training and Research Hospital, Department of Anesthesiology and Reanimation

    Ankara, 06010, Turkey (Türkiye)