Tiny study on nerve surgery for amputees halted early
NCT ID NCT04658368
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study aimed to measure how targeted muscle reinnervation (TMR) surgery affects quality of life and function in people who have had a major limb amputation. TMR was done either at the time of amputation or later. Only 2 people took part before the study was stopped early, so the findings are very limited.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Targeted muscle reinnervation (TMR) surgery
- What this could lead to
- If successful, this could show that TMR improves quality of life and function for people with major limb amputations.
- What could go wrong
- The study was terminated early with only 2 participants, so results are very limited and may not apply to others. It was also a small, single-center study.
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
-
2 people
The number who actually took part.
- Started
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Dec 2020
- Finished
-
Sep 2022
- 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.
Who is studied
Patients that have undergone (retrospective) or are scheduled to undergo (prospective) major limb amputation with primary or secondary TMR procedure at the UW. A control group of participants that have had major limb amputation at the UW without the TMR procedure will also be surveyed.
- 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: Study cohort * Retrospective * Underwent primary or secondary TMR with attending plastic surgeon at UW * Prospective * Patient with history of major limb amputation who is scheduled to undergo secondary TMR with attending plastic surgeon at UW * Patient who is scheduled to undergo primary major limb amputation with concurrent TMR Inclusion Criteria: Control Cohort * Patient with history of major limb amputation recruited from local clinics who has not been referred or seen for consultation for TMR by attending plastic surgeon at UW Exclusion Criteria: Study Cohort * Retrospective * Patient underwent TMR at another institution * Less than 6 months follow up * Less than 18 years of age * Enrolled in other studies relating to neuropathic pain * Undergoing radiation therapy * Incarcerated * Incomplete survey response * Non-English speaking (chosen PROMIS measures only in English) * Prospective * Less than 18 years of age * Cognitive impairment * Enrolled in other studies relating to neuropathic pain * Undergoing radiation therapy * Incarcerated * Non-English speaking (chosen PROMIS measures only in English) Exclusion Criteria: Control Cohort * Less than 18 years of age * Cognitive impairment * Enrolled in other studies relating to neuropathic pain * Undergoing radiation therapy * Incarcerated * Incomplete survey response * Major limb amputee seeking consultation for TMR * Non-English speaking (chosen PROMIS measures only in English)
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Wisconsin
Madison, Wisconsin, 53792, United States
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