RecruitingNot Applicable

Myopia Preventing With Distance-image Screen

China100 participantsStarted 2022-10-01

Plain-language summary

This study is for testing the efficacy and safety of distance-image screens for preventing myopia in children for 12 month. Each subjects would be asked to paired test the ocular parameters between before and after 12-month distance-image screens.

Who can participate

Age range

6 Years – 12 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * (1) Must be 6\~12 years old; * (2) Must be best corrected visual acuity \< logMAR: 0.1; * (3) Spherical Equivalence (SE) must be -1.00\~ + 6.00 Diopter (D), * (4) Spherical Equivalence (SE) must have changed \> 1.25 Diopter (D) in the recent 2 years; * (5) Must be astigmatism \<1.75 Diopter (D); * (6) Must be anisometropia \<1.75 Diopter(D). Exclusion Criteria: * (1) Strabismus disease; * (2) Amblyopia disease; * (3) Cataract disease; * (4) Glaucoma disease; * (5) Severe dry eye disease; * (6) Cannot use distance-image screen for 12 month; * (7) Other severe diseases that would effect the use of distance-image screen.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Changes of ocular axial length (mm)

Timeframe: 12-month

Changes of refractive error (D)

Timeframe: 12-month

Trial details

NCT IDNCT06088225

SponsorBeijing Airdoc Technology Co., Ltd.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2024-12-31

Contact for this trial

QIU JENNY, MD

+8618510386815 kkaiqiu@126.com

View on ClinicalTrials.gov More Myopia, Progressive trials

Who can participate

Age range

6 Years – 12 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.