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A Registry Study to Assess Photobiomodulation in Dry Age-Related Macular Degeneration (EUROLIGHT) (EUROLIGHT) - Trial NCT06351605

Access comprehensive clinical trial information for NCT06351605 through Pure Global AI's free database. This phase not specified trial is sponsored by LumiThera, Inc. and is currently Recruiting. The study focuses on Dry Age-related Macular Degeneration. Target enrollment is 500 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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Trial Details
ClinicalTrials.gov โ€ข NCT06351605
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A Registry Study to Assess Photobiomodulation in Dry Age-Related Macular Degeneration (EUROLIGHT) (EUROLIGHT)
A Multi-Center Registry Study to Assess the Safety and Effectiveness of Photobiomodulation in Participants With Dry Age-Related Macular Degeneration (EUROLIGHT)

Study Focus

Valeda Light Delivery System

Observational

device

Sponsor & Location

LumiThera, Inc.

Oslo, Norway

Timeline & Enrollment

N/A

Sep 01, 2023

Dec 01, 2026

500 participants

Primary Outcome

Best-Corrected Visual Acuity (BCVA)

Summary

The EUROLIGHT study is being conducted to collect real life data for the safety and
 effectiveness of PBM in dry AMD, in routine clinical practice both retrospectively and
 prospectively.

ICD-10 Classifications

Peripheral retinal degeneration
Corneal degeneration
Hereditary retinal dystrophy
Optic atrophy in diseases classified elsewhere
Disorders of choroid and retina

Data Source

ClinicalTrials.gov

NCT06351605

Device Trial