NCT06662162Recruiting
Microcurrent Stimulation Therapy for Intermediate to Advanced Nonexudative Age-related Macular Degeneration
Microcurrent Stimulation Therapy for Intermediate to Advanced Nonexudative Age-related Macular Degeneration (i-SIGHT2): a Multicentre, Randomised, Sham-controlled, Double-masked, Clinical Device Trial.
Source: ClinicalTrials.gov · Last updated 26 Aug 2026
Brief summary (registry, in English)
The goal of this clinical trial is to characterize the safety and effectiveness of the i-Lumen AMD transpalpebral microcurrent device and therapy in patients with intermediate to advanced nonexudative AMD. Participants will: * Undergo an initial loading regimen, followed by 7 maintenance over the course of 11 months. * Participants will return monthly through Month 14 (3 months post-last treatment) for evaluation and monitoring.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- First submitted
- 25 Oct 2024
- Start date
- 7 May 2025
- Primary completion date
- 31 Mar 2027
- Lead sponsor
- i-Lumen Scientific AUS PTY LTD
- Diseases
- Macular degeneration
- NCT number
- NCT06662162
What you commit to
- Study type: Interventional
- Planned participants: 100
- From 7 May 2025 to the primary completion date, 31 Mar 2027
- 13 sites in 4 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Treatment with photobiomodulation (PBM) therapy or short pulse laser within 12 months prior to screening.
Other illness
- Any implanted electrical device(s) including deep brain stimulator, hearing or visual implants (i.e., cochlear implant, auditory brainstem implant, retinal prostheses), and/or cardiac defibrillator/pacemaker.
- Known severe allergy to fluorescein dye.
- History of seizure disorders, chronic migraines and/or cluster headaches.
- Other conditions which pre-dispose to chorioretinal atrophy such as inherited retinal dystrophy (i.e., Stargardt's disease, Best's disease, pattern dystrophy, central areolar choroidal dystrophy, etc.).
- History of intravitreal injections for GA (e.g., Syfovre or Izervay).
- Glaucoma requiring ≥3 medications and/or drops per day, or history of trabeculectomy.
- History of any kind of intraocular surgery, excluding cataract surgery performed ≥3 months from Screening.
- History of yttrium aluminium garnet (YAG) laser posterior capsulotomy \<1 month from Screening.
- History of amblyopia.
Lab values
- Uncontrolled diabetes, defined as glycated haemoglobin (HbA1c) \>10% (13.3 mmol/L).
Other
- Implanted metallic device within 20 cm of the Treatment electrode (study eye(s)) and/or the grounding electrode (base of the hairline on the back of the neck).
- Current tobacco or tobacco-related product use or history within the past 5 years of heavy smoking (defined as, on average, more than half a pack of cigarettes per day).
- Medical diagnosis of severe dry eye defined as requiring either artificial tears more than six (6) times a day or prescription drops (i.e., Restasis, Xiidra, or Cequa).
- History and/or evidence of diabetic retinopathy in either eye as assessed by CF, fundus fluorescein angiography (FA), and OCT, to be confirmed by the Central Reading Centre.
- History and/or evidence of exudative AMD in the study eye as assessed by CF, FA (or OCT-A ), and OCT, to be confirmed by Central Reading Centre.
- GA involving the foveal centre, as assessed by the Central Reading Centre using AF and OCT.
- Visually significant cataracts and/or visually significant posterior capsular opacification.
Who the study is looking for
- Presence of at least one large druse \>125 microns in diameter due to AMD.
- BCVA letter score of 35 to 70 letters (inclusive) (Snellen equivalent 6/12 to 6/60 \[20/40 to 20/200\])
Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers
Sites (13)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Cerulea Coordinator of this site? Confirm its status | East Melbourne | Australia | Active, not recruiting |
| Queens University Belfast / Belfast City Hospital Coordinator of this site? Confirm its status | Belfast | United Kingdom | Recruiting |
| King's College Hospital Coordinator of this site? Confirm its status | London | United Kingdom | Recruiting |
| London North West University Healthcare Coordinator of this site? Confirm its status | Middlesex | United Kingdom | Recruiting |
| Sunderland Eye Infirmary Coordinator of this site? Confirm its status | Sunderland | United Kingdom | Recruiting |
| Auckland Eye Limited Coordinator of this site? Confirm its status | Remuera | New Zealand | Recruiting |
| Retina Associates of Cleveland Coordinator of this site? Confirm its status | Beachwood | United States | Recruiting |
| Texas Retina Associates Coordinator of this site? Confirm its status | Fort Worth | United States | Recruiting |
| University Retina & Macula Associates Coordinator of this site? Confirm its status | Lemont | United States | Recruiting |
| Retina Consultants PC Coordinator of this site? Confirm its status | Manchester | United States | Recruiting |
| Retina Consultants San Diego Coordinator of this site? Confirm its status | Poway | United States | Recruiting |
| Sierra Eye Associates Coordinator of this site? Confirm its status | Reno | United States | Not yet recruiting |
| Tyler Retina Research Insitute Coordinator of this site? Confirm its status | Tyler | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.