Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT06667037
NA

Orthokeratology and 0.01% Atropine Sequential Treatment for Myopia Control

Sponsor: Zhongshan Ophthalmic Center, Sun Yat-sen University

View on ClinicalTrials.gov

Summary

The purpose of this multicenter randomized clinical trial is to evaluate the myopia control effect of orthokeratology and 0.01% atropine sequential treatment in children and adolescents, as compared to continuous treatment with orthokeratology.

Official title: Myopia Control Effect of Orthokeratology and 0.01% Atropine Sequential Treatment in Children and Adolescents: A Multicenter Randomized Controlled Trial

Key Details

Gender

All

Age Range

8 Years - 15 Years

Study Type

INTERVENTIONAL

Enrollment

194

Start Date

2024-09-21

Completion Date

2027-03-31

Last Updated

2025-02-26

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Ortho-k lenses

Ortho-k lenses will be administered nightly.

DRUG

0.01% Atropine

0.01% Atropine will be administrated twice a day with an interval of about 12 hours. Drop into the conjunctival sac and immediately compress the lacrimal sac of the inner canthus for 2-3 minutes.

Locations (1)

Zhongshan Ophthalmic Center Sun Yat-Sen University

Guangzhou, Guangdong, China