Study of PEMF to Evaluate VPT and Thermal Sensory in Subjects With Diabetic Peripheral Neuropathy

Regenesis Biomedical

Status

Completed

Conditions

Diabetic Peripheral Neuropathy

Treatments

Device: Active Provant Therapy System

Device: Inactive (sham) Provant Therapy System

Study type

Interventional

Funder types

Industry

Identifiers

NCT03077893

RBI.2017.001

Details and patient eligibility

About

A study to demonstrate the effectiveness of PEMF treatment compared to sham treatment in changing Vibration Perception Threshold (VPT) and Thermal Sensory (QST) in patients with diabetic peripheral neuropathy (DPN) when treatment is administered twice daily through 120-day period.

Full description

Multi-center, sham-controlled, double-blind, enriched enrollment, randomized withdrawal clinical trial conducted on subjects with bilateral symmetrical diabetic peripheral neuropathy. Eligible subjects will include those between 22 and 80 years of age with Type 1 or Type 2 diabetes having persistent pain, numbness, tingling, or burning in both feet despite treatment. Eligible subjects will receive two active treatment devices (one for each foot, to allow simultaneous treatment) and treat at home, twice daily for 60 days after which they will return to the clinic at Day 61 for a response assessment. Subjects that are determined to be responders at Day 61 (subjects that achieve a 1-point decrease in the average pain score over the last 24 hours using the Numeric Pain Rating Scale (NPRS)) will be randomized 1:1 to either active treatment or inactive sham devices and will continue treating through Day 120. Subjects that are determined to be non-responders at Day 61 will continue treating with the active devices given at enrollment and will return to the clinic at Day 75 and Day 91 for a response assessment. If a subject is determined to be a responder at Day 75, they will be randomized 1:1 to receive either active treatment or inactive sham and will continue treating through Day 120. If a subject is determined to be a responder at Day 91, they will be randomized 1:1 to receive either active treatment or sham and will continue to treat through Day 120. If a subject continues to be a non-responder at Day 91 they will be terminated from the study.

Enrollment

44 patients

Sex

All

Ages

22 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subject age is greater than or equal to 22 years and less than 80 years of age.
Subject has documented Type 1 or Type 2 diabetes mellitus (receiving insulin, diet controlled, or taking parenteral hypoglycemic agents)
Subject is on a stable antidiabetic regimen (medication and/or diet) to control their diabetes for at least 30 days prior to Screening.
Subject has an HbA1c <10% at Screening or within 2 months of Screening.
Subject has daily pain attributed to bilateral symmetrical Diabetic Peripheral Neuropathy with numbness, tingling, and/or burning based on clinical judgement for at least 6 months prior to screening.
Subject's pain or discomfort from DPN is identifiable.
Subject is in pain Phase 2, 3, or 4 as per the Phasing of Neuropathy Scale.
Subjects average pain over the last 24 hours is ≥3 based on the 11-point Numeric Pain Rating Scale (NPRS) at the Screening Visit.
Subject has adequate lower extremity pulse in both feet and no intermittent claudication.
Subject is able to ambulate independently without assistive devices.
Subject is willing and able to give written informed consent and to comply with all parts of the study protocol.
Female subjects must be post-menopausal, surgically sterile, abstinent, or practicing (or agrees to practice) an effective method of birth control if they are sexually active for the duration of the study (Effective methods of birth control include prescription hormonal contraceptives, intrauterine devices, double-barrier methods, and/or male partner sterilization).

Exclusion criteria

Subject is in pain Phase 1 or 5 as per the Phasing of Neuropathy Scale.
Subject has an active, open ulcer on the lower extremities.
Subject has peripheral vascular disease defined as absence of more than one foot pulse per foot and/or ABI <0.8 and >1.4 and/or history of angioplasty or peripheral bypass surgery within 6 months of the Screening Visit.
Subject has venous insufficiency as classified by the Venous Insufficiency Classification System of grade C6.
Subject has undergone nerve decompression surgery on the lower extremities.
Subject has a history of previous kidney, pancreas, cardiac transplantation, or severe renal disease.
Subject has been diagnosed with non-diabetic chronic inflammatory neuropathic disease (e.g. end stage renal disease, hepatitis C, chemotherapy induced neuropathy, known connective tissue disease, systemic lupus).
Subject has peripheral vascular disease requiring revascularization of lower limb or amputation or evidence of ulcer amputation.
Subject has clinically significant cardiovascular disease within 6 months prior to screening (unstable or poorly controlled hypertension, transient ischemic attack, MI, unstable angina, arrhythmia, any heart surgery, stent placement, heart disease).
Subject has a history of any uncontrolled medical illness that in the Investigators judgment places the subject at unacceptable risk for receipt of PEMF therapy.
Subject requires or anticipates the need for surgery of any type or travel during the treatment period.
Subject has a total foot depth (most inferior aspect of the medial malleolus to the plantar aspect of the foot when residing on a treatment pad) of >8 cm.
Subject has received any investigational drug or device within 30 days prior to the Screening Visit or within 6 weeks prior to the Screening Visit for long acting lidocaine injection products.
Subject has used systemic corticosteroids within 3 months of the Screening Visit.
Subject has a history of malignancy within the past 5 years other than successfully treated non-metastatic basal cell or squamous cell carcinomas of the skin in the treatment area and/or localized in situ carcinoma of the cervix.
Subject has a serious psychosocial co-morbidity.
Subject has a history of drug or alcohol abuse, as confirmed by urine drug screen, within one year prior to the Screening Visit.
Subject has an implanted pacemaker, defibrillator, neurostimulator, spinal cord stimulator, bone stimulator, cochlear implant, or other implanted device with an implanted metal lead(s).
Subject is currently pregnant or planning on becoming pregnant prior to Day 121.
Subject has previously treated with PROVANT® Therapy System within 60 days on the lower extremity.
Subject is unwilling or unable to follow study instructions or comply with the treatment regimen, diary documentation, and study visits.
Subject has pain from any other source that can confuse the assessment of the pain associated with DPN.
Subject has a clinically significant foot deformity (Charcot's syndrome or club foot).
Subject has received nerve blocks for neuropathic pain within 4 weeks of the Screening Visit.
Subject has been diagnosed with mononeuropathy.
Subject has a skin condition that could alter their sensation.
Subject has had a previous surgery to the spine or lower extremity with residual symptoms of pain or difficulty with movement.
Subject has moderate or severe arthropathy (RA, OA, Gout) that causes discomfort during casual walking or stair climbing.