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Gabapentin in postamputation phantom limb pain: a randomized, double-blind, placebo-controlled, cross-over study
Margaret Bone1, Peter Critchley, Donal J Buggy
1Departments of Anaesthesia and Pain Management, University Hospitals of Leicester NHS Trust, Leicester General Hosptial, Leicester, UK.
Regional Anesthesia and Pain Medicine
|October 10, 2002
Summary
Gabapentin significantly reduced phantom limb pain compared to placebo in a randomized trial. While effective for pain, it did not show significant improvements in mood, sleep, or daily activities.
Area of Science:
- Neurology
- Pain Management
- Clinical Pharmacology
Background:
- Phantom limb pain affects a significant portion of amputees and is challenging to manage.
- Neuropathic pain conditions often respond to gabapentin.
- Evaluating gabapentin's efficacy for phantom limb pain is crucial.
Purpose of the Study:
- To assess the analgesic efficacy of gabapentin in patients experiencing phantom limb pain.
- To compare gabapentin monotherapy against placebo in a controlled study.
Main Methods:
- A randomized, double-blind, placebo-controlled, cross-over study involving patients with phantom limb pain.
- Gabapentin dosage was titrated up to 2400 mg daily, with a 6-week treatment period and a 1-week washout.
- Pain intensity was measured using the visual analog scale (VAS), with secondary measures including sleep, mood (HAD scale), and daily activities (Bartel Index).
Main Results:
- Gabapentin therapy resulted in a significantly greater reduction in VAS pain intensity difference compared to placebo (P = .03).
- No significant differences were observed between gabapentin and placebo for rescue medication use, sleep interference, depression, or daily living activities.
- Gabapentin was generally well-tolerated with minimal adverse effects reported.
Conclusions:
- Gabapentin monotherapy demonstrated superior efficacy over placebo in alleviating postamputation phantom limb pain after six weeks.
- No significant improvements were noted in mood, sleep, or activities of daily living, though a type II error is possible for these outcomes.