Closed Loop Spinal Cord Stimulation for Complex Regional Pain Syndrome

Status Not yet recruiting

Clinical Trial Summary

The primary purpose of this study is to determine the differences in response to treatment of complex regional pain syndrome with a closed-loop spinal cord stimulator if applied in the early phases (acute or subacute) versus the chronic phase.

Clinical Trial Description

After being informed about the study and the potential risks, all patients given written informed consent will be organized into group 1 (acute or subacute) and group 2 (chronic). They will undergo a trial period with a temporary spinal cord stimulator for 7 days. After the trial period, if the provider determines the device improved the patient's pain and function, the permanent device will be implanted. The patient will fill out an outcomes packet at baseline, end of trial period, 3 months and 6 months. There will also be a blood draw to evaluate prolactin levels, which are associated with stress and pain, at baseline, end of trial period, and 3 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06421350
Study type	Interventional
Source	Scripps Health
Contact	Julie C McCauley
Phone	585-554-7122
Email	mccauley.julie@scrippshealth.org
Status	Not yet recruiting
Phase	N/A
Start date	June 2024
Completion date	June 2026

View Details

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