TMS for Complex Regional Pain Syndrome

Launched by STANFORD UNIVERSITY · Apr 28, 2017

Keywords

ClinConnect Summary

This clinical trial is investigating a treatment called Transcranial Magnetic Stimulation (TMS) for people suffering from Complex Regional Pain Syndrome (CRPS), a condition that causes severe pain and other symptoms in a specific area of the body. The study aims to see if TMS can help reduce pain and improve overall well-being compared to a sham (placebo) treatment. Participants will receive TMS once daily for two days and will be monitored for two weeks to see if they feel better and how long the relief lasts.

To be eligible for this study, participants must be between 18 and 70 years old and have been diagnosed with CRPS for at least three months. They should also have a certain level of pain that meets the study's criteria. However, individuals with certain medical conditions, like those with metal implants, a history of epilepsy, or pregnancy, cannot participate. If you join the trial, you can expect to undergo TMS treatment and follow-up assessments to track your pain and symptoms. This study is currently recruiting participants of all genders, so if you or someone you know is interested, it could be a chance to explore a new treatment option.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Age 18-70
• • Diagnosis of CRPS (complex regional pain syndrome) for at least 3 months
• • Average pain level reported on Numerical Rating Scale meets entry criteria
• • Ability to perform the experimental task and procedures.
• Exclusion Criteria:
• • MRI contraindication (metal implants or devices, claustrophobia)
• • TMS Contraindication (eg metal implant or devices near the site of stimulation)
• • History of epilepsy
• • History of a psychological or psychiatric disorder that would interfere with study procedures, at the discretion of the researcher.
• • Neurologic illness that would interfere with brain integrity
• • Current medical condition or medication use that would interfere with study procedures or data integrity, at the discretion of the researcher.
• • Currently pregnant or planning to become pregnant.
• • On going legal action or disability claim.