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RecruitingNCT03137472

TMS for Complex Regional Pain Syndrome

Transcranial Magnetic Stimulation (TMS) for Complex Regional Pain Syndrome (CRPS)

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Stanford University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICETranscranial Magnetic Stimulation (TMS)The Magventure TMS stimulator will be used to perform intermittent theta burst followed by high frequency Transcranial Magnetic Stimulation (TMS).

Timeline

Start date
2017-04-24
Primary completion
2026-06-29
Completion
2026-06-29
First posted
2017-05-02
Last updated
2025-05-13

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03137472. Inclusion in this directory is not an endorsement.

TMS for Complex Regional Pain Syndrome (NCT03137472) · Clinical Trials Directory