Comparison of 10 kHz SCS Combined With CMM to CMM Alone in the Treatment of Neuropathic Limb Pain

Painful Diabetic Neuropathy Clinical Trial

— SENZA-PDN  

Official title:

A Post-Market, Multicenter, Prospective, Randomized Clinical Trial Comparing 10 kHz Spinal Cord Stimulation (HF10™ Therapy) Combined With Conventional Medical Management to Conventional Medical Management Alone in the Treatment of Chronic, Intractable, Neuropathic Limb Pain

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03228420
• Other study ID #: CA2016-5
• Status: Active, not recruiting
• Phase: N/A
• Start date: July 20, 2017
• Est. completion date: December 1, 2022

Study information

• Verified date: July 2021
• Source: Nevro Corp
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This post-market study is being conducted to document comparative safety, clinical effectiveness, and cost-effectiveness of the addition of HF10™ therapy to CMM compared with CMM alone in subjects with chronic, intractable, neuropathic lower limb pain due to diabetic neuropathy (Painful Diabetic Neuropathy or PDN). This study is a multi-center, prospective, randomized comparison of the two treatments.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 430
• Est. completion date: December 1, 2022
• Est. primary completion date: May 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 22 Years and older

Eligibility

Inclusion Criteria:

1. Have been clinically diagnosed with painful diabetic neuropathy (PDN) of the lower limbs.

2. Average pain intensity of = 5 out of 10 cm on the VAS in the lower extremities at enrollment.

3. Have stable neurological status.

4. Be on a stable analgesic regimen.

5. Be 22 years of age or older at the time of enrollment.

6. Be an appropriate candidate for the surgical procedures required in this study.

7. Be capable of subjective evaluation, able to read and understand English-written questionnaires, and able to read, understand and sign the written informed consent in English.

8. Be willing and capable of giving informed consent.

9. Be willing and able to comply with study-related requirements, procedures, and scheduled visits.

Exclusion Criteria:

1. Have a diagnosis of a lower limb mononeuropathy, have had a lower limb amputation, or have large (=3 cm) and/or gangrenous ulcers of the lower limbs.

2. Have a BMI = 40.

3. Currently prescribed a daily opioid dosage > 120 mg morphine equivalents.

4. Have a medical condition or pain in other area(s), not intended to be treated in this study.

5. Have a current diagnosis of a progressive neurological disease such a multiple sclerosis, chronic inflammatory demyelinating polyneuropathy, rapidly progressive arachnoiditis, brain or spinal cord tumor, central deafferentation syndrome, Complex Regional Pain Syndrome, acute herniating disc, severe spinal stenosis and brachial plexus injury.

6. Have a current diagnosis or condition such as a coagulation disorder, bleeding diathesis, platelet dysfunction, low platelet count, severely diminished functional capacity due to underlying cardiac/pulmonary disease, symptomatic uncontrolled hypertension, progressive peripheral vascular disease or uncontrolled diabetes mellitus that presents excess risk for performing the procedure.

7. Have failed prior SCS, dorsal root ganglion (DRG) stimulation, or peripheral nerve stimulation (PNS) trials for chronic intractable pain.

8. Have significant spinal stenosis, objective evidence of epidural scarring and/or any signs or symptoms of myelopathy.

9. Any previous history of surgery on the posterior elements (laminectomy, posterior fusion) resulting in a compromised epidural space.

10. Be benefitting from an interventional procedure and/or surgery to treat lower limb pain.

11. Have an existing drug pump and/or another active implantable device such as a pacemaker.

12. Have a condition currently requiring or likely to require the use of diathermy or MRI that is inconsistent with Senza system guidelines in the Physician's Manual.

13. Have either a metastatic malignant neoplasm or untreated local malignant neoplasm.

14. Have a life expectancy of less than one year.

15. Have a local infection at the anticipated surgical entry site or an active systemic infection.

16. Be pregnant or plan to become pregnant during the study. Women of childbearing potential who are sexually active must use a reliable form of birth control, be surgically sterile, or be at least 2 years post-menopausal.

17. Have within 6 months of enrollment a significant untreated addiction to dependency producing medications, alcohol or illicit drugs.

18. Be concomitantly participating in another clinical study.

19. Be involved in an injury claim under current litigation.

20. Be a recipient of Social Security Disability Insurance (SSDI).

21. Have a pending or approved worker's compensation claim.

22. Have evidence of an active disruptive psychological or psychiatric disorder or other known condition significant enough to impact perception of pain, compliance with intervention and/or ability to evaluate treatment outcome.

Related Conditions & MeSH terms

• Diabetic Neuropathies
• Painful Diabetic Neuropathy

Intervention

Device:
• Senza HF10 Therapy
Senza 10kHz Spinal Cord Stimulation

Other:
• CMM
Conventional Medical Management

Locations

Country	Name	City	State
United States	Coastal Orthopedics	Bradenton	Florida
United States	Duke University Medical Center	Durham	North Carolina
United States	Advanced Pain Management	Greenfield	Wisconsin
United States	Georgia Pain Care	Stockbridge	Georgia

Sponsors (1)

Lead Sponsor	Collaborator
Nevro Corp

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Composite of Safety and Effectiveness	Difference between treatment groups in responder rates in subjects without a clinically meaningful neurological deficit compared with baseline. Responder is defined as a subject who has at least 50% reduction in lower limb pain from Baseline as measured by a 10 cm Visual Analog Scale (VAS).	3 months
Secondary	Pain Scores of 3 or Less	Difference between the treatment groups in proportion of subjects with a lower limb pain VAS score = 3 cm.	3 months
Secondary	Crossover Rates	Difference between the treatment groups in crossover rates. Subjects who meet pre-specified criteria may elect to crossover to the other treatment arm at 6-month follow-up.	6 months
Secondary	Responder Rates	Difference between the treatment groups in responder rates. Responder is defined as a subject who has at least 50% reduction in lower limb pain from Baseline as measured by a 10 cm Visual Analog Scale (VAS).	6 months
Secondary	Remitter Rates	Difference between the treatment groups in the proportion of remitters (remission is defined as having a lower limb pain VAS score of = 3.0 cm for at least 6 months).	6 months
Secondary	Neurological Assessment	Difference between the treatment groups in the proportion of subjects with overall improvement from baseline in neurological assessment (motor, sensory, reflex).	3 months
Secondary	Neurological Assessment	Difference between the treatment groups in the proportion of subjects with overall improvement from baseline in neurological assessment (motor, sensory, reflex).	6 months
Secondary	Health-related Quality of Life	Difference between the treatment groups in changes in health-related quality of life as assessed by the EuroQol Five Dimensions questionnaire (EQ-5D-5L).	6 months
Secondary	Hemoglobin A1c	Difference between the treatment groups in the average percentage change from baseline in HbA1c levels.	6 months