Recruiting

High-Frequency SCS

Sponsor:

University of Nebraska

Code:

NCT06480786

Conditions

Peripheral Arterial Disease

Painful Diabetic Neuropathy

Diabetes Mellitus, Type 2

Chronic Pain

Spinal Cord Stimulation

Eligibility Criteria

Sex: All

Age: 19 - 70+

Healthy Volunteers: Not accepted

Interventions

Spinal cord stimulation

Sham stimulation

Study Details

Brief summary:

Peripheral arterial disease (PAD) affects over 230 million adults worldwide and is a highly morbid, costly, and disabling condition. Ischemic leg pain drives disability in PAD patients and results from oxygen supply-demand mismatch, autonomic dysfunction, and muscle breakdown. This leg pain, which is unresponsive to traditional pharmacotherapy, limits the patient's tolerance to exercise, which is an important disease-modifying intervention. Spinal cord stimulation is a well-established therapy for medically intractable pain, including painful diabetic neuropathy (PDN) and ischemic pain, but is not part of the standard-of-care for PAD despite limited promising clinical data. Early studies used first-generation, tonic stimulation devices, but with these it was impossible to perform sham-controlled trials to test the treatment. Since then, new types of waveform treatments, including high-frequency spinal cord stimulation (SCS), have been shown to be more effective in the treatment of intractable pain. While high-frequency SCS is approved for PDN treatment, it has never been tested in the treatment of claudication pain from PAD.

This study will enroll up to 15 participants between the ages of 19 and 89 who have PAD and PDN and are successfully implanted with a permanent SCS. Twelve weeks after SCS implantation, participants will receive two weeks of stimulation and two weeks of sham intervention, in random starting order. Blood flow, blood pressure, skin oxygen levels, and participant reported pain int the lower extremities will be assessed before SCS implantation, 12 weeks after SCS implantation and during each of the treatment periods. Participants will also complete a quality of life survey at the same time points. Comparisons of these measurements with the baseline and post-implantation measurements to determine the effects of SCS.

Conditions

Peripheral Arterial Disease

Painful Diabetic Neuropathy

Diabetes Mellitus, Type 2

Chronic Pain

Spinal Cord Stimulation

Study ID

NCT06480786

Start date

Dec 18, 2024

Status verified date

Oct, 2025

Completion date

Jul, 2027

Anticipated

Primary completion date

Jan, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 19 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • 19 years to 89 years old
  • Diagnosed diabetes mellitus
  • Signs or symptoms of neuropathy and maximum baseline visual-analog pain scale ≥ 5 cm and peripheral arterial disease (diagnosed by ankle-brachial index < 0.90 or vascular imaging studies) with claudication and exertion-induced visual-analog pain scale ≥ 6 cm for a minimum of 3 months
  • Successful spinal cord stimulator (SCS) trial (>50% relief of chronic lower extremity pain) and will have a new permanent SCS placed prior to study intervention

Exclusion Criteria:

  • Uncontrolled psychological or psychiatric disorder
  • Inability to hold antithrombotic therapy per the American Society of Regional Anesthesia guidelines
  • Non-healing wounds
  • Gangrene
  • Critical limb ischemia
  • Prior lower extremity amputation
  • Inability to adhere to study follow-up
  • Mechanical spine instability based on flexion/extension radiographs of the lumbar spine
  • Prior or current spinal cord stimulator implant

Study Design

Enrollment

15 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Active Spinal Cord Stimulation

Therapeutic spinal cord stimulation titrated at 12 weeks post operative at standard clinical practice.

sham comparator: Sham Stimulation

Sub-threshold low frequency spinal cord stimulation to provide no analgesic benefit but serve as a sham control.

Interventions

Spinal cord stimulation

active spinal cord stimulation

Sham stimulation

Sham stimulation

Primary outcome measure

  • High-frequency Spinal Cord Stimulation Effect on Analgesia [ Time Frame: Baseline, 12 week follow-up after permanent spinal cord simulator, week 14 intervention #1 , week 16 intervention #2 ]

Central Contacts and Locations

Central contacts

Locations

University of Nebraska Medical Center

Recruiting

Omaha, Nebraska, United States, 68198

Contacts

More Information

Sponsor

University of Nebraska

Last update posted

Oct 22, 2025

Last verified

Oct, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Nebraska on 2025-10-22.