Spinal Add-On may ease phantom pain after amputation
NCT ID NCT07565662
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether adding dexmedetomidine to standard spinal anesthesia could lower the chance of acute neuropathic pain after a leg amputation. Thirty adults having elective lower limb amputation were split into two groups: one got the standard anesthetic plus a placebo, the other got the standard anesthetic plus dexmedetomidine. The main focus was on pain relief and nerve block duration, with a secondary look at neuropathic pain using a screening tool at 48 hours.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- dexmedetomidine
- What this could lead to
- If it works, this could offer a simple way to reduce phantom limb pain after amputation.
- What could go wrong
- This is a small, early-stage trial with only 30 participants, so results may not apply to everyone. The pain reduction may be modest or not significant.
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
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30 people
The number who actually took part.
- Started
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Apr 2025
- Finished
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Oct 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 to 65 years
- Sex
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Anyone
- Healthy volunteers
-
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: * Patients scheduled for elective supra- or infracondylar lower limb amputation * Age 18 to 65 years * ASA physical status I-III * Acceptance of neuraxial anesthetic technique Exclusion Criteria: * Patient refusal of anesthetic procedure * Prolonged coagulation times * Anatomical abnormalities of the spine * ASA IV classification * Atrioventricular block grade 2 or 3 without pacemaker * Neurological deterioration (Glasgow score less than 8) * Hemodynamic instability
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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
-
Hospital Regional de Alta Especialidad Dr. Juan Graham Casasus
Villahermosa, Tabasco, 86126, Mexico
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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