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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age4-14
SponsorFangbiao Tao

About this trial

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.

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Ear acupoint pressure pellet intervention group
  • Atropine intervention group
  • Joint intervention Group
  • control group

Treatment groups

380 Participants
are divided into 4 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Fangbiao Tao

Lead sponsor

Anhui Medical University

Sponsor institution