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Recruiting NCT06452914

NCT06452914 Clinical Outcomes Related to Treatment of Distal Symmetric Polyneuropathy Using Semiconductor Embedded Therapeutic Socks

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Clinical Trial Summary
NCT ID NCT06452914
Status Recruiting
Phase
Sponsor Endocrine Research Solutions
Condition Diabetic Neuropathy
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2024-06-11
Primary Completion 2025-06

Trial Parameters

Condition Diabetic Neuropathy
Sponsor Endocrine Research Solutions
Study Type INTERVENTIONAL
Phase N/A
Enrollment 80
Sex ALL
Min Age 18 Years
Max Age 79 Years
Start Date 2024-06-11
Completion 2025-06
Interventions
Semiconductor Embedded Therapeutic SocksPlacebo Socks

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Brief Summary

Distal symmetric polyneuropathy, also known as diabetic neuropathy, is the most common neurological complication of diabetes and a main cause of morbidity. The condition leads to gradual loss of function of the longest nerve fibers that limits function and decreases quality of life. Symptoms present distally and symmetrically in toes and feet. Symptoms of the neurologic disability include sensory loss, risk of foot ulcers and limb amputations and pain. The condition is not generally considered reversible, and condition management aims to slow progression and prevent complications. According to estimates from the International Diabetes Federation, diabetic neuropathy affected approximately 425 million people in 2017, with projections indicating a rise to 628 million by 2045. Despite the high prevalence of this condition, it is commonly misdiagnosed and has limited treatment options. There are multiple phenotypes of diabetic neuropathy, with the most common form being distal symmetric sensorimotor polyneuropathy, which is what we will be focusing on in this study. The proposed study seeks to evaluate the effectiveness of a non-compressive therapeutic socks throughout a 12-week course of rehabilitation for managing distal symmetric polyneuropathy. Outcome measures will be collected at standard intervals and compared with pre-treatment measures to evaluate effectiveness of treatment.

Eligibility Criteria

Inclusion Criteria: * Patients diagnosed with mild to moderate Diabetic Neuropathy with a score between 2 and 7 out of 10 on the MNSI upon clinical examination and assessment. * Patients reporting symptoms of Diabetic Neuropathy * Patients age 18-79 * Patients who are willing and able to adhere to follow-up schedule and protocol guidelines * Patients who are willing and able to sign corresponding research subject consent form Exclusion Criteria: * Patient has a history of neurodegenerative conditions, including multiple sclerosis or Parkinson's disease * Patient has chronic pain conditions unrelated to diabetic neuropathy, including spinal stenosis, low back pain, and sciatica * Patient has auto-immune or auto-inflammatory diseases other than Diabetic Neuropathy, including Multiple Sclerosis or Lyme Disease * Patient has experienced a stroke * Patient has any type of paralysis * Patients with a score less than 2 and greater than 7 out of 10 on the MNSI upon clinical examination and ass

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