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Starting soon Not applicable

Evaluation of an Electric Stimulator for Medical Use by Personal (LRTPM1) for Visual Function in Early to Intermediate Dry Age-Related Macular Degeneration

NCT07700147 · tracked via the Priya Life Science South Korea tracker
Sponsor
Nu Eyne Co., Ltd
Phase
Not applicable
Started
2026-07-09
Last updated
2026-07-13

Condition(s) studied

Dry Age-Related Macular DegenerationAMD

Investigational drug(s) / intervention(s)

Transcutaneous Electrical StimulationSham Transcutaneous Electrical Stimulation

Transcutaneous Electrical Stimulation: The active intervention uses transcutaneous electrical stimulation (TES) delivered by the investigational personal-use electric stimulator (LRTPM1). Electrodes are attached to the ocular and periocular area, and the device delivers pulsed electrical stimulation. Participants will apply the assigned device once daily for 30 minutes over a 12-week treatment period.

Sham Transcutaneous Electrical Stimulation: The sham device is identical in appearance to the active investigational device but does not provide active electrical stimulation. Participants will apply the assigned sham device once daily for 30 minutes over a 12-week treatment period.

Study summary

The goal of this clinical trial is to evaluate the efficacy and safety of an electric stimulator for medical use by personal (LRTPM1) in patients with early to intermediate dry age-related macular degeneration.

The main questions this study aims to answer are:

* Does the investigational device improve visual function, as assessed by best corrected visual acuity and contrast sensitivity?
* What treatment-emergent adverse events occur during the study?

Participants will:

* Be randomized to receive either active stimulation or sham stimulation
* Apply the assigned investigational device at home once daily for 30 minutes over a 12-week treatment period
* Visit the study site for eye examinations and safety assessments
* Return for a follow-up visit 4 weeks after the end of treatment

Eligibility

Sex
ALL
Min age
50 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Participants aged 50 years or older 2. Participants diagnosed with early or intermediate dry age-related macular degeneration 3. Participants with best corrected visual acuity measured by the ETDRS visual acuity chart of 20/200 or better and 20/30 or worse 4. Participants who have voluntarily decided to participate in the study and have provided written informed consent. Exclusion Criteria: 1. Participants with atrophy involving the foveal center with a diameter of 175 micrometers or greater in at least one eye, as observed by fundus examination or fundus autofluorescence imaging 2. Participants with exudative age-related macular degeneration in at least one eye, as observed by fundus examination or optical coherence tomography (OCT) 3. Participants with a history of intraocular injection therapy or macular laser treatment, including focal laser photocoagulation or photodynamic therapy 4. Participants with retinal or choroidal diseases other than early or intermediate age-related macular degeneration that may affect the study results, including diabetic retinopathy, retinal artery occlusion, retinal vein occlusion, central serous chorioretinopathy, optic neuritis, or uveitis 5. Participants who have undergone vitrectomy due to retinal disease, or cataract surgery within 1 month prior to screening 6. Participants with ocular media opacity or other conditions that, in the investigator's opinion, may make ophthalmic imaging difficult to interpret, including cataract, vitreous opacity, or vitreous hemorrhage 7. Participants with uncontrolled chronic systemic diseases, including diabetes mellitus or chronic kidney disease, or a history of malignancy, except for cases with no recurrence within the past 5 years and no history of chemotherapy 8. Participants with autoimmune diseases, including Sjögren's syndrome, rheumatoid arthritis, systemic lupus erythematosus, or Graves' disease 9. Participants with severe hearing impairment, sensory abnormalities, or cognitive impairment that may make it difficult to properly perform the study procedures or recognize or report adverse events 10. Participants who are hypersensitive to orbital nerve stimulation and are unable to receive treatment 11. Participants with a history of drug or alcohol abuse 12. Participants diagnosed with psychiatric disorders, including depression, schizophrenia, bipolar disorder, or dementia 13. Participants who have participated in another clinical trial within 30 days prior to screening 14. Participants who are considered to have other contraindications to use of the investigational medical device, including underlying cardiac disease, seizure-related disorders, implanted metal or electronic devices in the head or neck area including deep brain stimulators, unexplained pain, implanted or wearable pacemakers, or other conditions listed in the product precautions and contraindications. Dental implants are exempt. 15. Participants who, in the opinion of the investigator, are deemed inappropriate for participation in the study 16. Female participants of childbearing potential who do not agree to use medically accepted contraception during the study period. Medically accepted methods of contraception include condoms, oral contraceptives used consistently for at least 3 months, injectable or implantable contraceptives, or intrauterine devices.

Primary outcome measure(s)

  • Change in Best Corrected Visual Acuity (BCVA) Measured by ETDRS Letter Score — Baseline, Week 2, Week 6, Week 12, Week 16
    Change from baseline in best corrected visual acuity (BCVA) measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity chart. BCVA will be recorded as an ETDRS letter score. Higher scores indicate better visual acuity.
  • Change in Contrast Sensitivity — Baseline, Week 2, Week 6, Week 12, Week 16
    Change from baseline in contrast sensitivity as measured using a contrast sensitivity chart at four spatial frequencies (3, 6, 12, and 18 cycles/degree). Contrast sensitivity is recorded as a level value from 1 to 8, with higher recorded values indicating better ability to perceive contrast differences.

Trial sites (3)

FacilityCityRegionStatus
Korea University Ansan Hospital Ansan Gyeonggi-do
Seoul National University Hospital Seoul Jongno-gu
Asan Medical Center Seoul South Korea
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07700147 on ClinicalTrials.gov ↗ ← All trials in South Korea