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NCT Number: NCT06667037

Orthokeratology and 0.01% Atropine Sequential Treatment for Myopia Control

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.

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Key information

Age range

8 year–15 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 8-15 years old.
  • Spherical equivalent refractions (SERs) -0.50 to -6.00 Dioptres (D) and astigmatism less than -1.5 D in both eyes, anisometropia less than 1.5 D.
  • Best corrected visual acuity (BCVA) equal to or better than 20/25 in both eyes.
  • Bilateral intra-ocular pressure < 21mmHg.
  • Normal binocular and stereoscopic visual function.
  • Participants and their guardians' understanding and acceptance of random allocation of grouping.

Exclusion criteria

  • Manifest strabismus, except for intermittent tropia.
  • Ocular or systemic diseases which may affect vision or refractive error.
  • Previous use of myopia control without washout, including atropine, myopia control spectacles, myopia control contact lenses.
  • Other contraindications.

Treatment and study plan

ortho-k lenses

Device

Ortho-k lenses will be administered nightly.

0.01% atropine

Drug

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.

Primary outcomes

  1. Axial length change

    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).

Secondary outcomes

  1. Proportion of rapid myopia progression

    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.

  2. Axial length change

    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).

  3. Incidence of adverse events

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Xiao Yang, Professor

CONTACT

[email protected]

86-13760766303

Yin Hu, Doctor

CONTACT

[email protected]

86-18664783831

Sponsors and collaborators

Lead sponsor

Zhongshan Ophthalmic Center, Sun Yat-sen University

Other

Collaborators

  • Henan Provincial People&#39;s Hospital
  • People&#39;s Hospital of Guangxi
  • Tianjin Medical University Eye Hospital

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Oct 31, 2024
Registry last updated
Feb 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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