Zhongshan Ophthalmic Center Sun Yat-Sen University
Guangzhou, Guangdong, 510060, China
Location status: Recruiting
Location contact
Xiao Yang, Professor
CONTACT
Yin HU, PhD
CONTACT
NCT Number: NCT06667037
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.
Interested in participating?
Request Info8 year–15 year
All sexes
Interventional
Not applicable
Guangzhou, Guangdong, 510060, China
Location status: Recruiting
Xiao Yang, Professor
CONTACT
Yin HU, PhD
CONTACT
Myopia constitutes a major threat to vision health globally for its increasing prevalence and irriversible blinding complications. It is crucial to effectively intervene subjects with progressive myopia to reduce risks of myopic pathologies in later life.
Orthokeratology (ortho-k) is the first-line intervention for myopia control, with an efficacy of slowing axial elongation by 43-63%. However, the efficacy decreases over time. Sequential treatment strategy, which switches myopia control interventions at some intervals, has a potential to increase myopia control efficacy regarding the whole treatment period, compared to applying one intervention throughout. However, there lacks evidence supporting the benefit of this treatment strategy.
The purpose of this study is to evaluate the effectiveness of orthokeratology and 0.01% atropine sequential treatment on myopia control in children and adolescents, as compared to continuous treatment with orthokeratology, using a multicenter randomized controlled trial design. Subjects will be randomly assigned into either ortho-k and 0.01% atropine sequential treatment group or ortho-k continuous treatment group. Their axial length will be monitored over two years. Changes in axial length in the two groups will be compared.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ortho-k lenses will be administered nightly.
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.
Time frame: From baseline to the end of treatment at 25 months
Axial length change (mm) is characterized as the difference between 25-month follow-up visit and baseline values. The IOLMaster or Lenstar are used to measure axial length (mm).
Time frame: From baseline to the end of treatment at 25 months
Proportion of rapid myopia progression means the rate of cumulative axial growth ≥0.50 mm at 25 months) after intervention.
Time frame: From baseline to 3, 6, 9, 12, and 19 months.
Axial length change (mm) is characterized as the difference between 3, 6, 9, 12, and 19 months follow-up visit and baseline values. The IOLMaster or Lenstar are used to measure axial length (mm).
Time frame: From baseline to 25 months.
Incidence of adverse events is the rate of adverse events over the study period for subjects in both arms.
Contact information is provided by the study sponsor or research team.
Xiao Yang, Professor
CONTACT
Yin Hu, Doctor
CONTACT
Zhongshan Ophthalmic Center, Sun Yat-sen University
Other
Myopia Control Effect of Orthokeratology and 0.01% Atropine Sequential Treatment in Children and Adolescents: A Multicenter Randomized Controlled Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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