Can freezing nerves stop phantom limb pain?
NCT ID NCT06908538
First seen Jun 27, 2026 · Last updated Aug 27, 2026 · Updated 2 times
Summary
This study is tracking how well freezing nerves during amputation surgery works to reduce pain after the operation and phantom limb pain. Researchers will follow 2000 adults who are having an arm or leg amputated. The goal is to see if this nerve-freezing technique is safe and helpful.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cryoablation (nerve freezing via a probe)
- What this could lead to
- If successful, this could provide a way to reduce severe pain after amputation, including phantom limb pain, without long-term medication.
- What could go wrong
- This is an observational registry, not a controlled trial, so it cannot prove the treatment works. The nerve block is temporary (weeks to months), and pain may return. Risks include procedural complications.
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.
- Participants
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About 2,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2025
- Expected to finish
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Apr 2035
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Subjects who have or will have an amputation procedure.
- 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: * Patients who have or will have an amputation procedure; * Patients who are willing and capable of providing informed consent; * Patients whose age is 18 years or above, or of legal age to give informed consent specific to state and national law. Exclusion Criteria: * Women of childbearing potential who are, or plan to become, pregnant during the time of the study; * Other medical, social, or psychological conditions that in the opinion of the Investigator precludes the subject from appropriate consent or adherence to the protocol.
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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
6 sites. 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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Berkshire Medical Center
RECRUITINGPittsfield, Massachusetts, 01201, United States
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Elliot Hospital
RECRUITINGManchester, New Hampshire, 03101, United States
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Medical College of Wisconsin/Froedtert Hospital
RECRUITINGMilwaukee, Wisconsin, 53226, United States
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NYU Langone Health
RECRUITINGNew York, New York, 10017, United States
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Ohio State University
RECRUITINGColumbus, Ohio, 43210, United States
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Prisma Health - Upstate
RECRUITINGGreenville, South Carolina, 29605, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can bionic limbs feel real? a trial tests touch feedback for amputees
- Can a common anesthetic dampen phantom limb pain?
- Can tiny electrodes give amputees a better grip on bionic limbs?