Board-certified Pain Specialists
At PA Pain & Spine Institute, we provide spinal cord stimulation (SCS) for chronic pain that hasn’t improved with medications or other treatments.
Spinal cord stimulator treatment is designed to help patients who are experiencing:
✅ Chronic back or leg pain that has not improved with prior treatments
✅ Numbness, tingling, or burning pain in the feet or lower legs due to diabetic neuropathy
✅ Failed back surgery syndrome or persistent post-surgical pain
✅ Complex regional pain syndrome (CRPS)
✅ Radiculopathy or nerve pain that travels into the lower extremities
Joint Pain & Arthritis Specialists
It typically affects most people at some point in their life due to injuries or overuse. It can make movement, various activities and daily life a challenge. Some typical causes of pain in your joints or arthritis are:
✅ Broken Bones
✅ Fibromyalgia
✅ Sprains
✅ Tendinitis
✅ Autoimmune Conditions
✅ Overuse or Injury
✅ Brusitis
Spinal cord stimulation is a neuromodulation therapy that works by delivering mild, targeted electrical pulses to the spinal cord. These pulses interrupt pain signals before they reach the brain, effectively reducing or eliminating the perception of chronic pain. In most cases, the therapy does not cause pain to disappear entirely; rather, it replaces disruptive pain with a mild, manageable sensation, or in many modern systems, no sensation at all.
The treatment is designed for patients whose pain has persisted despite conservative care, including medications, physical therapy, and interventional procedures such as injections. Because it is reversible and adjustable, SCS is considered a low-risk option relative to repeat surgery, and it can be trialed temporarily before a permanent device is implanted.
At PA Pain & Spine Institute, Dr. Bozak evaluates each patient thoroughly before recommending SCS. The evaluation includes a review of imaging, prior treatment history, and the specific nature and location of the patient’s symptoms. This careful selection process is essential, as patient-specific factors significantly influence long-term outcomes.
Spinal cord stimulation is one of the most extensively studied interventional pain therapies in the published literature. Our approach at PA Pain & Spine Institute focuses on preserving function and avoiding the risks, recovery time, and long-term complications that come with open surgery. Below are the evidence-based options we offer.

Fluoroscopy-guided epidural steroid injections deliver corticosteroid medication directly to the affected spinal level, reducing inflammation around the compressed nerve roots. For patients experiencing acute stenosis-related leg pain or neurogenic claudication, this can provide meaningful short-term relief and allow for improved function while a longer-term treatment plan is developed.
*This is done outpatient and does not require anesthesia

Minimally invasive neuromodulation therapy, outpatient trial phase followed by permanent implantation if successful, fully reversible and adjustable, strong alternative to repeat spinal surgery
*This is done outpatient and does not require anesthesia in most cases

Anti-inflammatory medications and topical agents are used to manage acute symptom flare-ups and support recovery alongside interventional treatments. Our team monitors all medications carefully and adjusts based on your response and overall health over time.
*This is done outpatient and does not require anesthesia

When chronic pain is accompanied by secondary facet joint arthritis, which is a common occurrence in degenerative lumbar disease, medial branch blocks and radiofrequency ablation can interrupt pain signals from the affected facet joints directly. Radiofrequency ablation provides longer-duration relief by applying controlled heat to the targeted sensory nerve.
*This is done outpatient and does not require anesthesia in most cases
Traditional open spine surgery requires general anesthesia, large incisions, significant muscle dissection, and often a hospital stay. Recovery can take several weeks to months. SCS, by contrast, involves a minimally invasive trial phase and, if successful, a permanent implantation through a small incision, typically in under two hours, without disturbing the surrounding muscles or major spinal structures. Patients go home the same day and are usually able to return to light daily activities within one to two weeks. Additionally, SCS is fully reversible, which is not the case with most surgical interventions.
Schedule a consultation if you experience:
Early evaluation allows for a precise diagnosis and more targeted care. Left untreated, chronic neuropathic pain can progress and lead to worsening neurological symptoms, including significant weakness and loss of function.
SCS is appropriate for carefully selected patients. In general, strong candidates are those who have a confirmed diagnosis of a condition with an established SCS indication, have pursued and not found sufficient relief through conservative treatments, and do not have medical or psychological contraindications to the procedure.
Patients who tend to be strong candidates include:
Dr. Bozak evaluates each patient individually based on their diagnosis, imaging findings, treatment history, and overall health. A preoperative psychological evaluation is also a standard component of the candidate selection process, consistent with current SCS clinical guidelines.
Spinal cord stimulation has received FDA clearance for the treatment of painful diabetic peripheral neuropathy, and it is one of the most significant emerging indications for the therapy. If you experience numbness, tingling, or burning pain in your feet that has not responded adequately to medications, SCS may be an appropriate next step. Dr. Bozak will evaluate whether your specific presentation makes you a candidate.
The SCS system consists of two main components: a thin lead containing small electrodes, and a pulse generator that powers the system. The lead is positioned in the epidural space near the spinal cord, and the pulse generator is implanted under the skin, typically near the lower back or abdomen. The entire system is internal and not visible once implanted.
Because the therapy is fully adjustable, stimulation parameters can be reprogrammed non-invasively after implantation to optimize pain relief as the patient’s condition evolves over time.
Before committing to a permanent implant, patients undergo a trial period lasting approximately 7 to 10 days. During the trial, temporary leads are placed and connected to an external device worn outside the body. This allows the patient and Dr. Bozak to evaluate whether the therapy provides meaningful relief before any permanent commitment is made.
If the trial results in at least 50% reduction in pain, or meaningful functional improvement, the patient is considered a responder and can proceed to permanent implantation. Research from a large real-world study of 505 SCS trials conducted between 2022 and 2024 found that 86.1% of patients achieved trial success, and 76.6% of those who received a permanent implant maintained significant improvement at follow-up.
Research insight: A real-world cohort study of 505 patients (Interventional Pain Institute, 2022–2024) found that 86.1% achieved trial success and 76.6% of permanently implanted patients maintained significant improvement at follow-up. Patients with diabetic neuropathy showed the highest success rate at 83.3%.
(Gheith R, et al. Journal of Pain Research. 2025. doi: 10.2147/JPR. PMC12672166.)
Permanent SCS implantation is an outpatient procedure performed under fluoroscopic guidance. The leads are precisely positioned at the target spinal level, and the pulse generator is implanted through a small incision. The entire procedure typically takes between one and two hours. Most patients return home the same day and resume light daily activities within one to two weeks.
Importantly, the procedure is reversible. If a patient’s circumstances change, or if the therapy is no longer providing adequate relief, the device can be removed or reprogrammed accordingly.
Symptoms that may indicate SCS candidacy depend on the underlying condition:
Imaging:
Research insight: A multicenter study of 505 patients treated with SCS showed an 86.1% trial success rate, with diabetic neuropathy patients demonstrating the highest success rate at 83.3% [Gheith et al., Journal of Pain Research, 2025].
Our goal is not simply to manage pain. We work to find the right solution for each patient’s specific anatomy, symptoms, and goals, with a clear preference for approaches that preserve function and avoid the risks of major surgery.
Patients benefit from:
Spinal cord stimulation has received FDA clearance for a range of chronic pain conditions. Furthermore, recent regulatory expansions have broadened the approved indications, particularly for patients living with neuropathic pain related to diabetes. The conditions below are among those treated with SCS at PA Pain & Spine Institute.
SCS is one of the most well-established treatments for persistent back and leg pain, particularly in patients who have already undergone spinal surgery without adequate relief. This condition, commonly referred to as failed back surgery syndrome (FBSS) or persistent spinal pain syndrome (PSPS), is one of the primary indications for SCS therapy and has been supported by decades of peer-reviewed evidence.
One of the most significant recent developments in SCS therapy is the FDA’s expanded approval for painful diabetic peripheral neuropathy (DPN). DPN is a progressive nerve condition caused by chronically elevated blood glucose levels, most commonly affecting the feet, lower legs, and hands. Patients often describe symptoms as numbness, tingling, or a burning sensation that begins in the toes and moves upward, and which can become severe enough to interfere with sleep, mobility, and daily function.
Approximately 50% of adults with diabetes will develop peripheral neuropathy during their lifetime, and for many, medications provide only partial relief or produce intolerable side effects. SCS now represents a non-opioid, non-medication option that has demonstrated meaningful and durable outcomes in this population. Notably, the real-world cohort study referenced above found that patients with diabetic neuropathy had the highest SCS trial success rate of any diagnostic group at 83.3%.
CRPS is a chronic pain condition typically affecting an arm or leg following injury, surgery, or nerve damage. It is characterized by disproportionate, sustained pain, changes in skin color and temperature, and swelling. SCS is a recognized treatment for CRPS and is supported by both FDA clearance and multiple published clinical guidelines.
Radiculopathy, or pain that radiates from the spine into the extremities along a nerve root pathway, is another condition for which SCS provides meaningful relief. Patients with radiculopathy often describe sharp, shooting, or electric pain that travels into the buttocks, legs, or feet, and which has not adequately responded to injections or physical therapy.
The information on this page is for general educational purposes only and does not constitute medical advice. Treatment recommendations are based on individual clinical evaluation. Individual results may vary, and no specific outcomes are guaranteed. This content does not create a provider-patient relationship.
