Complex Regional Pain Syndrome
Conditions
Keywords
RSD, SCS, CRPS
Brief summary
To demonstrate that spinal cord stimulator has an effect on sympathetic function (the one that give us the fight and flight response). Therefore, if the spinal cord stimulator has an effect on sympathetic function, the responses from CRPS patients to different stimuli will differ significantly pre and post SCS implant. If CRPS patients exhibit autonomic, CRPS patients could be stratified according to their sympathetic function pre-implant. It is expected that patients with a moderate/mild form of autonomic dysfunction will have better outcomes with the SCS.
Detailed description
Currently the mechanisms of Complex Regional Pain Syndrome (CRPS) are poorly understood and stratification of either diagnosis or therapy is very weak. . There is a great need to develop and validate more objective methods to characterize and stratify CRPS that better diagnostic and therapeutic approaches are available. Spinal Cord Stimulation (SCS) has been used as the last resource to alleviate pain and re-establish function in CRPS patients. However, there is a disagreement over how it works. An underlying concept is that it works by modulating autonomic nervous system (ANS) activity. Therefore, ANS parameters could be useful to stratify patients. Our preliminary studies indicated that SCS has also an effect on blood pressure regulation and improves the CRPS patients' response to Valsalva maneuver -a test of autonomic function. The Autonomic Nervous System function in adult CRPS patients has not yet been studied. The only existing study of CRPS and autonomic function showed that 15% of the patients suffer from syncope and increased heart rate during upright position similar to same aged patients with postural tachycardia syndrome - a syndrome of autonomic dysfunction. It is unclear if autonomic dysfunction is present in CRPS patients because ANS activity is altered by chronic pain or whether or not ANS activity contributes to CRPS. Therefore, we proposed to study the autonomic function in CRPS patients by standardized autonomic function and to evaluate the effect of the SCS on autonomic function in CRPS patients before and after spinal cord stimulator implant. This is a 24 months study.
Interventions
OTHERAutonomic Function Assessment
Sponsors
Vanderbilt University Medical Center
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* CRPS patients meeting the inclusion criteria according to the International Association for the Study of pain task Force will be included in the study. * Age: 18 to 65. * Disease duration of at least 6 months. * History of unsuccessful long lasting therapies: physical therapy, transcutaneous electrical stimulation and medication.
Exclusion criteria
* Presence of current or past pulmonary, hepatic, renal disease, arthritis, hematopoietic, and neurological diseases not related to CRPS. * Anticoagulant therapy, cardiac pacemaker used. * Pregnancy test for females is positive.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in muscle sympathetic nerve activity | At baseline and within 2 years | Electrical neurography data from sympathetic nerves |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Heart rate | At baseline and within 2 years | Heart rate (bpm) |
| Blood pressure response | At baseline and within 2 years | Blood pressure (mmHg) |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORPeter Konrad, M.D.
Vanderbilt University
Outcome results
None listed