TMS for Complex Regional Pain Syndrome

Status Recruiting

Clinical Trial Summary

The aim of the current study is to assess the efficacy of TMS in the treatment of Complex Regional Pain Syndrome (CRPS). It is hypothesized that participants who receive TMS (Group 1) relative to sham treatment (Group 2) once daily for two days will demonstrate a greater improvement in CRPS-related pain and other associated symptomology (i.e., cognitive, emotional and physical) compared to baseline. Participants will be followed until they reach their baseline for two consecutive weeks to assess safety and duration of symptom alleviation.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03137472
Study type	Interventional
Source	Stanford University
Contact	Birute Gedrimaite
Phone	(650) 497-0485
Email	birute@stanford.edu
Status	Recruiting
Phase	N/A
Start date	April 24, 2017
Completion date	June 29, 2026

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