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Clinical Trials/NCT03259451
NCT03259451
Withdrawn
Not Applicable

Effectiveness of Repetitive Transcranial Magnetic Stimulation in the Treatment of Chronic Neuropathic Pain: Retrospective Study on a Cohort of 149 Patients at Rennes University Hospital, From January 2014 to December 2015

Rennes University Hospital1 site in 1 countrySeptember 26, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Neuropathic Pain
Sponsor
Rennes University Hospital
Locations
1
Primary Endpoint
Evaluation of the efficacy of rTMS in the treatment of chronic neuropathic pain in a short term
Status
Withdrawn
Last Updated
8 years ago

Overview

Brief Summary

A retrospective, monocentric, observational, descriptive, open study of a cohort of 149 patients from January 2014 to December 2015

Detailed Description

Neuropathic pain is a public health problem because of its prevalence reaching nearly 7% of the general population and the effectiveness of current treatments often remains incomplete: only 30-40% of patients are relieved of 50% of their pain by a pharmacological approach. As early as the 1990s, stimulation of the motor cortex by implanted electrodes made it possible to successfully treat certain chronic refractory neuropathic pain. In 1995 it was reported that the application of repeated shocks by transcranial magnetic stimulation of the motor cortex could induce an analgesic effect in a patient suffering from neuropathic pain. This technique has proved its analgesic efficacy after an induction treatment over 5 days, in the context of chronic pain (neuropathic or fibromyalgia), but all the patients are not responders and there is currently, Of predictive criteria for response. It seems important to continue studies on this non-medicinal, non-invasive therapy with no significant adverse effects.

Registry
clinicaltrials.gov
Start Date
September 26, 2016
End Date
December 31, 2017
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Rennes University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patient older than 18 years old with chronic neuropathic pain who are resistant to drug therapy for which treatment with rTMS is indicated between January 2014 and December 2015

Exclusion Criteria

  • Patient less than 18 years old
  • Pregnant woman
  • Non-neuropathic pain
  • Pain \<6 months
  • Unbalanced epilepsy
  • Patient with a contraindication for cerebral MRI (cochlear implant, ocular metallic foreign bodies, patient with a pacemaker, mechanical valve)
  • Psychiatric pathology
  • Person subject to major legal protection (safeguarding justice, guardianship, trusteeship), persons deprived of liberty

Outcomes

Primary Outcomes

Evaluation of the efficacy of rTMS in the treatment of chronic neuropathic pain in a short term

Time Frame: Day 7

Improvement of pain symptoms by at least 30% on the numerical scale

Evaluation of the efficacy of rTMS in the treatment of chronic neuropathic pain in a short term (≤ 1 month)

Time Frame: Month 1

Improvement of pain symptoms by at least 30% on the numerical scale

Secondary Outcomes

  • Evaluate the effectiveness of rTMS in the treatment of long-term chronic neuropathic pain (> 6 months)(Month 6)

Study Sites (1)

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