CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 9 enrolled
Drug / intervention
transcranial Direct Current Stimulation (tDCS): (Soterix ©)device
Likely dose
tDCS 2 mA applied to primary motor cortex contralateral to amputated limb for 20 minutesAI-extracted
Key inclusion· 4
  • Age >18 years
  • At least 3 months of phantom limb pain occurring at least once per week after complete healing of amputated limb
  • Average pain intensity ≥4 on numeric rating scale (0-10) in the previous week
  • Stable medication dosages for at least 2 weeks prior to enrollment if taking any medications
Key exclusion· 10
  • Ferromagnetic metal in head (plates, pins, bullets, shrapnel)
  • Implanted head electronic medical devices (cochlear implants)
  • Head injury with loss of consciousness ≥30 minutes or post-traumatic amnesia >24 hours
  • Uncontrolled epilepsy

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02627495
NCT02627495N/ACompleted

Predicting Pain Response to Transcranial Direct Current Stimulation for Phantom Limb Pain in Limb Amputees

Spaulding Rehabilitation Hospital·interventional·Posted Dec 11, 2015·Updated May 11, 2021

In Brief

A clinical study evaluating transcranial Direct Current Stimulation (tDCS): (Soterix ©) for Phantom Limb Pain. Completed, enrolled 9 participants across 1 site.

Detailed Summary

This study explores the effects transcranial Direct Current Stimulation (tDCS, Soterix ©) on Phantom Limb Pain for patients experiencing chronic phantom limb pain in open-label study design.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedDec 11, 2015
Enrollment StartDec 1, 2015
Primary CompletionNov 22, 2019
Study CompletionMar 9, 2021
TodayJul 2, 2026
Enrollment to primary: 4.0 yearsPosted 10.6 years ago

Interventions

transcranial Direct Current Stimulation (tDCS): (Soterix ©)device

Subjects will undergo tDCS stimulation. We will use electrodes of 35cm\^2, at an intensity of 2mA on the primary motor cortex contralateral to the amputated limb (or for bilateral amputees contralateral to the most painful side). The subject will undergo stimulation for 20 minutes. The subject will have 5 sessions of stimulation during a 1 week time period.