Noninvasive brain stimulation for treating amblyopia in adults
Official title: Multi-day Effect of Noninvasive Brain Stimulation in Adults With Amblyopia
Run by Midwestern University · NCT06712849 · Data updated 2026-11-12
This study is testing a new non-invasive brain stimulation method to see if it can help adults with amblyopia improve their vision.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 55 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Midwestern University Academic / other |
| Locations | 1 site (Downers Grove, Illinois) |
| Status | Recruiting |
| Started | May 1, 2024 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2028 |
| Registry record updated | December 12, 2024 |
| Trial ID | NCT06712849 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18 to 55 with a formal diagnosis of amblyopia.
✕Probably not a fit
Patients with a history of optic nerve disease, neurological conditions, or those with metal/electronic implants may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates the effectiveness of non-invasive brain stimulation, specifically high-frequency transcranial random noise stimulation, in treating adults with amblyopia. Participants will be randomly assigned to receive either active stimulation or sham stimulation over five consecutive days. The study aims to assess the impact of this intervention on neuronal plasticity in the visual cortex and its effects on visual perception and function. Researchers will measure various visual acuity parameters to evaluate the outcomes of the treatment.
Why it matters
Potential benefit: If successful, this approach could improve visual perception and function in adults suffering from amblyopia.
How similar studies have gone: While the approach of using non-invasive brain stimulation is relatively novel in the context of adult amblyopia, similar techniques have shown promise in other neurological and visual disorders.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults between 18 and 55 years of age * Formal diagnosis of amblyopia in one or both eyes of any etiology Exclusion Criteria: * History of optic nerve disease, including glaucoma and optic neuritis * History of neurological conditions, including demyelinating disease or stroke * Presence of metal or electronic implants in or on the body, including pacemakers * Taking medications that can affect normal neurological function, including antipsychotics, antiepileptics, and opioids
Where it's running
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Midwestern University Eye Institute
Downers Grove, Illinois, United States Recruiting
Study contacts
- Study coordinator: Arijit Chakraborty, PhD
- Email: achakr@midwestern.edu
- Phone: 630-960-3172
Similar studies
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This trial tests whether adding HD-tDCS to AR-based dichoptic therapy can improve vision in adults with anisometropic amblyopia.
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This study tests whether non-invasive brain stimulation (tDCS) can improve vision for children aged 4–14 with amblyopia who didn’t get enough help from patching.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.