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Clinical Trial Summary

This study will investigate the efficacy and safety of "deep" rTMS on neuropathic pain or fibromyalgia. It will be randomized and sham controlled and will last 3 months. Patients will be randomized to receive acctive rTMS or sham rTMS and will receive repeated rTMS sessions (5 daily sessions then one session per week then every 2 to 3 weeks for up to 10 weeks).


Clinical Trial Description

This double blind sham controlled parallel group bicenter study will assess the efficacy and safety of repeated sessions of deep rTMS using H coil in patients with neuropathic pain or fibromyalgia. Primary outcome will be % of pain relief at week 13. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06250491
Study type Interventional
Source Hospital Ambroise Paré Paris
Contact Nadine ATTAL
Phone 0033149095931
Email nadine.attal@aphp.fr
Status Recruiting
Phase N/A
Start date January 30, 2024
Completion date April 30, 2027

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