Complex Regional Pain Syndrome Clinical Trials

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Efficacy of Closed-Loop Spinal Cord Stimulation for Complex Regional Pain Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 18 years or older

• neuromodulation naive patients with unilateral CRPS type 1 or type 2 (defined by Budapest Criteria)

• pre-procedure psychological clearance

Locations
United States
California
Scripps Clinic Torrey Pines
RECRUITING
La Jolla
Contact Information
Primary
Julie C McCauley
mccauley.julie@scrippshealth.org
585-554-7122
Backup
Roslyn M Kackman
kackman.roslyn@scrippshealth.org
858-554-7122
Time Frame
Start Date: 2024-09-03
Estimated Completion Date: 2026-06
Participants
Target number of participants: 32
Treatments
Experimental: Acute and Subacute Phases of CRPS
Participants diagnosed with acute and subacute phases of CRPS will be assigned to this group.
Experimental: Chronic Phase of CRPS
Participants diagnosed with chronic CRPS will be assigned to this group.
Related Therapeutic Areas
Sponsors
Leads: Scripps Health

This content was sourced from clinicaltrials.gov