Transcranial Magnetic Stimulation (TMS) for CRPS

Completed · Not applicable

Conditions studied: Complex Regional Pain Syndrome (CRPS)

In brief

The purpose of this pilot study is to test the durability of response to Transcranial Magnetic Stimulation (TMS) for the symptoms of Complex Regional Pain Syndrome (CRPS). The investigators will test various methods of TMS for varying lengths of time in a pilot study to investigate what the clinical impact.

Key facts

Study ID

NCT02067273

Run by

Stanford University

People needed

20

Starts

2014-02-01

Expected to finish

2015-03-01

Last updated by the study team

2017-05-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 18 or older
• Diagnosis of CRPS (complex regional pain syndrome)
• Average pain level reported on Numerical Rating Scale meets entry criteria
• Ability to perform the experimental task and procedures.

You may not qualify if…

• 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.

Where it is running

• Stanford University School of Medicine — Palo Alto, California, United States

Full record on ClinicalTrials.gov

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