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NOT YET RECRUITING
NCT07047924
NA

A Clinical Trial Assessing the Safety and Effectiveness of Orthokeratology Lenses in Patients With Myopia and Myopic Astigmatism

Sponsor: Menicon Co., Ltd.

View on ClinicalTrials.gov

Summary

This is a prospective, multi-centre, single-arm clinical trial to evaluate the effectiveness and safety of MCOK-01 lenses in patients with myopia and myopic astigmatism who need dioptric correction. A maximum number of 220 participants are planned to be enrolled , with a minimum of 150 planned to complete the trial (30% dropout). All participants will be enrolled in Australia. Enrolled participants will wear the lenses every night for up to 12 months, removing them upon waking. 8 follow up visits will be completed during treatment, after: 1 day, 1 week, 2 weeks, 1 month, 3 months, 6 months, 9 months and 12 months of wearing the lenses.

Official title: A Prospective, Multi-centre, Single-Arm Clinical Trial of Orthokeratology Lenses (MCOK-01) in Subjects With Myopia and Myopic Astigmatism

Key Details

Gender

All

Age Range

6 Years - 40 Years

Study Type

INTERVENTIONAL

Enrollment

220

Start Date

2025-07-01

Completion Date

2026-12-01

Last Updated

2025-07-02

Healthy Volunteers

No

Interventions

DEVICE

MCOK-01

The investigational device is a Rigid Gas Permeable contact lenses for orthokeratology. MCOK-01 applied the reverse geometry design and adopted the lens material which possesses the highest oxygen permeability among all the materials for orthokeratology lens.

Locations (4)

Eyecare Kids

Hillsdale, New South Wales, Australia

UNSW School of Optometry and Vision Science

Sydney, New South Wales, Australia

Queensland University of Technology Optometry and Vision Science

Kelvin Grove, Queensland, Australia

The University of Melbourne Department of Optometry and Vision Sciences

Carlton, Victoria, Australia