Comparing Long-term Effectiveness of High Frequency and Burst Spinal Cord Stimulation

Over 100 million Americans suffer from chronic pain resulting in annual cost of roughly $635 billion. Limited treatments are available for this widespread disease. The data supporting these treatments lack generalizability to patients with more serious medical and psychological comorbidities who are often excluded from explanatory efficacy trials. This study aims to integrate randomized comparative effectiveness research with patient care. The investigators will randomize the patients and collect data using an open-source learning healthcare system already in use in the department to monitor patients' progress: Collaborative Health Outcomes Information Registry (CHOIR). CHOIR uses the National Institute of Health Patient Reported Outcomes Measurement Information System item banks for comparative metrics through computer adaptive testing. The investigators will leverage the advantage of this novel system to compare effectiveness of high frequency and burst spinal cord stimulation in improving pain and function in patients with chronic back and/or leg pain. Spinal cord stimulation is an effective treatment for chronic pain resulting in >50% pain relief in about half of the patients. Novel waveforms for spinal cord stimulation - high frequency and burst - increased the efficacy of this treatment even further. However, there is lack of data guiding decision making of the clinicians in choosing the best waveform in treating the patients with chronic pain. The proposed study will provide the clinicians with this evidence. Currently, data about safety and efficacy of these two novel waveforms is available for up to 24 months. The proposed research will provide data about effectiveness of these two modalities for at least 36 months. Moreover, this study will evaluate feasibility of integrating randomized comparative effectiveness research with patient care in Stanford Pain Management subspecialty clinic. CHOIR can then be applied for numerous future trials to advance knowledge in perioperative and pain medicine.

Stanford is currently not accepting patients for this trial.

Stanford Investigator(s):

Intervention(s):

  • device: High frequency spinal cord stimulation
  • device: Burst spinal cord stimulation

Eligibility


Inclusion Criteria:

   1. Adult English-speaking patient 18 years old or above

   2. Persistent pain in lower back and/or leg for more than six months

   3. Candidate for spinal cord stimulation (with either high frequency or burst waveforms)
   based on recommendations from Stanford Pain Management Center Neuromodulation
   Multidisciplinary Team Conference.

Exclusion Criteria:

   1. Motor weakness in neurological examination in lower body based on the assessment by
   treating pain physicians

   2. Previous failed spinal cord stimulation trial with either high frequency or burst
   waveforms

   3. Patient refusal

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Vafi Salmasi, MD.
6507250246
Not Recruiting

Our research team includes physicians, residents, medical students, research assistants, and volunteers. Our research topics include medical imaging, device validation,  mobile application development, and pharmaceutical trials.  

Some of the Neuro-Opthalmic concerns we investigate include Multiple Sclerosis, Optic Neuritis, IIH, and ICP.