NCT06229665

Study of Photobiomodulation to Treat Dry Age-Related Macular Degeneration (LIGHTSITEIIIB)

An Open-Label, Prospective, Multi-Center Extension Study to Assess the Long-Term Safety and Efficacy of Photobiomodulation (PBM) in Subjects With Dry Age-Related Macular Degeneration (AMD) (LIGHTSITE IIIB)
LumiThera, Inc.·Phase 2/3·ClinicalTrials.gov·device·Device trialRecruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
Valeda Light Delivery System
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
LumiThera, Inc.
Location
Beverly Hills,Palo Alto,Altamonte Springs,Hagerstown,Cherry Hill,New York,Durham,McAllen,Silverdale, United States of America
Timeline & enrollment
Phase
Phase 2/3
Start date
Oct 25, 2023
End date
Jun 01, 2025
Enrollment
75 participants
Primary outcome

Early Treatment Diabetic Retinopathy Study (ETDRS) Best-Corrected Visual Acuity (BCVA)

Summary

This study is an open-label, prospective, multi-center extension study on the continued use
 of photobiomodulation (PBM) in subjects with dry age-related macular degeneration (AMD) that
 participated in the CSP005 LIGHTSITE III study.

ICD-10 classifications
Peripheral retinal degenerationCorneal degenerationHereditary retinal dystrophyOptic atrophy in diseases classified elsewhereDisorders of choroid and retina
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06229665
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT06229665 through Pure Global AI's free database. This Phase 2/3 trial is sponsored by LumiThera, Inc. and is currently Recruiting. The study focuses on Dry Age-related Macular Degeneration. Target enrollment is 75 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.