Infrared Images for Spinal Cord Stimulation in Complex Regional Pain Syndrome Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorHospital for Special Surgery, New York

About this trial

The goal of this observational study is to compare thermal camera Forward Looking InfraRed (FLIR) images before and after spinal cord stimulation to evaluate the difference in sympathetic activity of the affected limb in patients with complex regional pain syndrome (CRPS). The main questions it aims to answer are:

Question 1: Can Infrared (FLIR) imaging be used to monitor the sympatholytic activity caused by Spinal Cord Stimulation (SCS) in patients with CRPS?

Question 2: Is there any correlation between the quantification of sympatholytic activity produced by Spinal Cord Stimulation (SCS) and measured by FLIR imaging with the outcome measures in patients with CRPS? Outcome measures include pain (NRS), CRPS Severity Score (CSS), and neuropathic pain score (painDETECT).

Participants will have an image of their feet taken perpendicularly with a 1-inch space from all four sides using a FLIR T420 or T62101 camera with 320\*240 resolution.

Participants will also complete questionnaires about the average pain, CRPS severity, and neuropathic pain.

Eligibility criteria

Qualifiers

The patient is between 18 and 85 years old

Providing CRPS diagnostic criteria by using the Budapest Clinical Diagnostic Criteria.

CRPS affecting unilateral lower extremity

The patient has had pain and other symptoms for more than 3 months

Disqualifiers

Patients with suspected disc herniation, spinal stenosis, myelopathy, and suspected radiculopathy in detailed examinations and examinations (MRI, CT).

Systemic or local infection

Coagulation disorders

History of allergy to contrast material

Trial design

Treatments tested in this trial

  • Forward Looking InfraRed Camera

Treatment groups

12 Participants
are divided into 1 treatment group