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Clinical Trial Summary

The purpose of this study is to compare the analgesic effectiveness of three modes of repetitive Transcranial Magnetic Stimulation (rTMS) in chronic neuropathic pain: - Classical rTMS stimulation - Deeper rTMS stimulation - Sham rTMS stimulation


Clinical Trial Description

Conduct of study: - Entry into the study: After informed consent, patients will be randomised. The physician responsible for conducting neurostimulation sessions will make the randomization via an interactive web response system (IWRS). Only this physician will have the knowledge of the group allocated to the patient. - Baseline : Patients, will record on a diary form, a daily Visual Numeric Scale(VNS) of Pain Intensity for 1 week. - Treatment sessions: after the baseline, sessions of neurostimulation will begin for seven weeks. - After the end of neurostimulation sessions, patients will be followed for 2 weeks. - Throughout their participation in the study, patients will plot on a diary form their daily VNS. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04936646
Study type Interventional
Source University Hospital, Grenoble
Contact Hasan HODAJ, MD
Phone 04-76-76-52-13
Email HHodaj@chu-grenoble.fr
Status Recruiting
Phase N/A
Start date July 16, 2021
Completion date December 1, 2024

See also
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