Neuroprosthetic device to improve diabetic neuropathy symptoms
Neuroprosthetic Device for Improving Issues Caused by Diabetic Neuropathy With Specifically Designed Neural Stimulation
This study tests whether a special device that uses electrical stimulation can help people with diabetic neuropathy feel better and improve their movement.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Institute Mihajlo Pupin Academic / other |
| Locations | 1 site (Belgrade) |
| Trial ID | NCT06471517 on ClinicalTrials.gov |
What this trial studies
This study investigates the use of a neuroprosthetic device that employs transcutaneous electrical stimulation to restore sensation in patients suffering from diabetic neuropathy. The approach focuses on enhancing sensory feedback and potentially alleviating neuropathic pain associated with nerve damage. Participants will be monitored for improvements in sensory function and overall mobility. The study aims to provide insights into the effectiveness of electrical stimulation in treating peripheral nerve damage caused by diabetes.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals diagnosed with polyneuropathy who can stand and walk unassisted and have sensory loss in their feet.
Not a fit: Patients with open ulcers on their feet, those who are pregnant, or individuals with certain psychological conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the quality of life for patients with diabetic neuropathy by restoring sensation and reducing pain.
How similar studies have performed: Other studies utilizing electrical stimulation for neuropathy have shown promising results, suggesting that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosed polyneuropathy * Ability to stand and walk unassisted. * Sensory loss in the feet Exclusion Criteria: * Open ulcers on the feet * Pregnancy * History of or current psychological diseases that include schizophrenia and major depression * Hypersensitivity to electrical stimulation
Where this trial is running
Belgrade
- Clinics for Endocrinology, Diabetes and Metabolic Diseases, Clinical Center of Serbia — Belgrade, Serbia (Recruiting)
Study contacts
- Principal investigator: Stanisa Raspopovic, PhD — Institute Mihajlo Pupin
- Study coordinator: Natalija Secerovic, PhD
- Email: natalija.katic@pupin.rs
- Phone: +381631268862
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.