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Clinical Trial Summary

Evaluate the safety and efficacy of transpalpebral microcurrent stimulation (MCS) therapy for patients with nonexudative (dry) age-related macular degeneration (AMD).


Clinical Trial Description

The i-Lumen(TM) AMD device is for in-office therapy use to deliver microcurrent electrical stimulation transpalpebrally (via the eyelid) for use by an ophthalmologist. The i-Lumen AMD device contains proprietary software with preset treatment algorithms and is calibrated at each session to the individual participant. Up to 30 enrolled participants will be randomized (2:1 active to sham ratio) and complete the initial 5-day loading treatment sessions. Participants completing the initial loading sessions will receive two (2) days of maintenance treatments and be following and be followed through the one (1) year time point. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05447650
Study type Interventional
Source i-Lumen Scientific, Inc.
Contact Meredith Mundy
Phone 408-440-7049
Email clinical@i-lumen.com
Status Recruiting
Phase N/A
Start date April 12, 2022
Completion date March 2024

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