Clinical Trial

Effects of Auricular Point Pressing With Pellets in Children With Insufficient Hyperopia Reserve

Not Yet Recruiting
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Summary
This project aims to address the trend of early onset and high myopia among children in China by focusing on insufficient hyperopia reserve, a key early warning indicator for myopia. A randomized controlled trial (RCT) will be conducted. The study will target children aged 4 to 14 with insufficient hyperopia reserve (equivalent spherical lens -0.50D to +0.75D). Through a prospective RCT design, the efficacy and safety of auricular point pressure therapy, low-concentration atropine eye drops, and their combination in delaying the onset of myopia will be systematically evaluated.
Trial Details
NCT Number NCT07475585
Lead Sponsor Fangbiao Tao
Conditions Myopia, Ear Acupressure Pellets, Hyperopia Reserve, Low-concentration Atropine Eye Drops, Eye Axis
Enrollment 380 participants
Start Date 2026-03-30
Primary Completion 2027-07-30 (estimated)
Study Completion 2027-07-30 (estimated)
Updated on ClinicalTrials.gov 2026-03-16