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Clinical Trial of Orthokeratology Lens (MCOK-01)

NCT06037850 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 390

Last updated 2025-02-07

No results posted yet for this study

Summary

A prospective, multicenter, randomized, controlled clinical trial of orthokeratology lens

Conditions

  • Myopia

Interventions

DEVICE

Test orthokeratology lens

Randomized to test orthokeratology lens worn during sleep every night

DEVICE

Control orthokeratology lens

Randomized to control orthokeratology lens worn during sleep every night

Sponsors & Collaborators

  • Menicon Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • Stan Isaacs · I & Vision Research Centre Pte. Ltd.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-07-29
Primary Completion
2024-10-31
Completion
2024-10-31

Countries

  • Singapore

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06037850 on ClinicalTrials.gov