New hope for amputees: Needle-Free pain relief without surgery?
NCT ID NCT07431424
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested two treatments for painful nerve growths (stump neuromas) that can occur after a leg amputation. 26 adults received either a steroid injection or a procedure using heat (radiofrequency ablation) guided by ultrasound. The goal was to see which treatment better reduces pain and improves daily life.
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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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26 people
The number who actually took part.
- Started
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Jan 2023
- Finished
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Feb 2024
- 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 65 years
- Sex
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Male participants only
- 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: * Participants aged 18 to 65 years. * Unilateral or bilateral traumatic lower extremity amputation. * Amputation level: transfemoral, transtibial, or Syme amputation. * Residual limb pain with a VAS score ≥ 4. * Willing and able to provide informed consent. * No injection to the distal stump and no surgery targeting the stump within the past 3 months. Exclusion Criteria: * Unwilling or unable to provide informed consent. * Conditions in which radiofrequency ablation and/or steroid injection are contraindicated, including inflamed or infected skin, impaired skin integrity at the procedure site, active bleeding at the site, unstable epilepsy or unexplained seizure history, uncontrolled diabetes mellitus, unstable acute cardiac arrhythmia or heart failure, or presence of a cardiac pacemaker. * History of allergy to the injected medications (e.g., local anesthetics and/or corticosteroids). * Psychiatric disorder or cognitive impairment that would prevent completion of study questionnaires.
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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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Gaziler Physical Medicine and Rehabilitation Training and Research Hospital
Ankara, Ankara, 06800, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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