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NCT05881655

Slow Myopia Progression With Different Irradiance Light

Status unknown NA Last updated 31 May 2023
What this trial tests

NA trial testing Airdoc Red Lighting Device in Myopia, Progressive in 75 participants. Status unknown.

Timeline
20 May 2023
Primary endpoint
30 May 2024
30 December 2025

Quick facts

Lead sponsorBeijing Airdoc Technology Co., Ltd.
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment75
Start date20 May 2023
Primary completion30 May 2024
Estimated completion30 December 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Beijing Airdoc Technology Co., Ltd.

Who can join

Adults 6 to 12, any sex, with Myopia, Progressive. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

It is a prospective clinical control study on red light control myopia with specail design spectacles for 75 children in 3 groups. Study Groups with two different powers of 0.6 mW and 1.2 mW at wavelength of 650nm. The control group is to wear the same brand and design spectalces as those two study groups. In addition, the progression of myopia is usually accompanied by the changes in a variety of ocular parameters, such as refractive error, reduced submacular choroidal thickness, and prolonged length of the ocular axis length.The goal is to test which power (1.2mW and 0.6mW) is better in myopic children for 3 month's follow-up and also to test how to get better result with the increaing or decreasing lighting power for the total 6 month follow-up results .

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Myopia, Progressive

Currently open trials in the same condition.

Other Beijing Airdoc Technology Co., Ltd. trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05881655.

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