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Slow Myopia Progression With Different Irradiance Light

Sponsored by Beijing Airdoc Technology Co., Ltd.

About this trial

Last updated 2 years ago

Study ID

Airdoc MPC

Status

Recruiting

Type

Interventional

Phase

N/A

Placebo

No

Accepting

18-75 Years
6 to 12 Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Started 2 years ago

What is this trial about?

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 .

What are the participation requirements?

Yes

Inclusion Criteria

- 6~12 years old

- Refractive Error of Myopia within -0.50 D~-5.00 D, Anisometropia less or equal to 2.00D, The best corrected vision acuity is better or equal to 0.8 (decimal record).

- Written consent formed with supervisions and children with 6 month follow-up.

No

Exclusion Criteria

- Photophobia or allergy to any cycloplegic eyedrops (such as tropcaine, cyclopentolate).

- Lesions in fundus or any part of eyeball with abnormal corrected vision such as keratoconus.

- Strabisumus with angles large or equal to 5 prism dioper.

- With other myopia control device such as atropine, Orthokeratology, Misight lens or other myopia control device.

Locations

Location

Status

Recruiting