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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
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

Full criteria on ClinicalTrials.gov

Sites (13)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Cerulea
Coordinator of this site? Confirm its status
East MelbourneAustraliaActive, not recruiting
Queens University Belfast / Belfast City Hospital
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BelfastUnited KingdomRecruiting
King's College Hospital
Coordinator of this site? Confirm its status
LondonUnited KingdomRecruiting
London North West University Healthcare
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MiddlesexUnited KingdomRecruiting
Sunderland Eye Infirmary
Coordinator of this site? Confirm its status
SunderlandUnited KingdomRecruiting
Auckland Eye Limited
Coordinator of this site? Confirm its status
RemueraNew ZealandRecruiting
Retina Associates of Cleveland
Coordinator of this site? Confirm its status
BeachwoodUnited StatesRecruiting
Texas Retina Associates
Coordinator of this site? Confirm its status
Fort WorthUnited StatesRecruiting
University Retina & Macula Associates
Coordinator of this site? Confirm its status
LemontUnited StatesRecruiting
Retina Consultants PC
Coordinator of this site? Confirm its status
ManchesterUnited StatesRecruiting
Retina Consultants San Diego
Coordinator of this site? Confirm its status
PowayUnited StatesRecruiting
Sierra Eye Associates
Coordinator of this site? Confirm its status
RenoUnited StatesNot yet recruiting
Tyler Retina Research Insitute
Coordinator of this site? Confirm its status
TylerUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.