PDN Post Market, Multicenter, Prospective, Global Clinical Study
The purpose of this post-market study is to evaluate the real-world experience of Nevro's Spinal Cord Stimulation (SCS) therapy in patients with chronic, intractable leg pain due to painful diabetic neuropathy (PDN). This is a multicenter, prospective, observational global study, that will partner diabetes management teams with pain physicians to provide an interdisciplinary treatment regimen for PDN patients. Outcomes will be assessed via standardized assessments.
Conditions:
🦠 Diabetic Neuropathy, Painful
🗓️ Study Start (Actual) 5 July 2022
🗓️ Primary Completion (Estimated) October 2026
✅ Study Completion (Estimated) March 2027
👥 Enrollment (Estimated) 497
🔬 Study Type INTERVENTIONAL
📊 Phase NA
Locations:
📍 Anchorage, Alaska, United States
📍 Bloomfield, Michigan, United States
📍 Ypsilanti, Michigan, United States
📍 Columbus, Ohio, United States
📍 Edmond, Oklahoma, United States
📍 Milwaukie, Oregon, United States
📍 Roanoke, Virginia, United States

📋 Eligibility Criteria

Description

    Inclusion Criteria:

      Inclusion Criteria:

      • 1. Have been clinically diagnosed with diabetes, according to the local country diabetes association guidelines, as well as painful diabetic neuropathy (PDN) of the lower limbs refractory to conventional medical management.
      • 2. Average pain intensity (over the last 7 days) of ≥5 out of 10 cm on the Visual Analog Scale (VAS) in the lower limbs at enrollment/baseline.
      • 3. The clinical decision has been made to provide treatment using the Nevro Spinal Cord Stimulation that includes 10 kHz therapy prior to enrollment in the study.
      • 4. Be willing and capable of giving written informed consent.
      • 5. Be willing and able to comply with study-related requirements and procedures and attend all scheduled visits.

      Exclusion Criteria:

      • 1. Have a diagnosis of a lower limb mononeuropathy (e.g., causalgia and tibial or peroneal neuropathies), have had a lower limb amputation other than toes, or have large (≥3 cm) and/or gangrenous ulcers of the lower limbs
      • 2. Have a medical condition or diagnosis that is inconsistent with Nevro's SCS System guidelines in the Physician's Manual for the relevant country, or as per standard clinical practice.
      • 3. Have a medical condition or pain in other areas, not intended to be treated in this study, that could interfere with study procedures, accurate pain reporting, and/or confound the evaluation of study endpoints, as determined by the Investigator (such as primary headache, fibromyalgia, post-herpetic neuralgia, osteoarthritis, peripheral vascular disease, or small vessel disease).
Ages Eligible for Study: 18 Years to N/A (ADULT, OLDER_ADULT)
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: No

🗓️ Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

  • First Submitted 11 February 2022
  • First Submitted that Met QC Criteria 25 March 2022
  • First Posted 31 March 2022

Study Record Updates

  • Last Update Submitted that Met QC Criteria 12 January 2024
  • Last Update Posted 17 January 2024
  • Last Verified January 2024