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Long-term Efficacy of Orthokeratology Contact Lens Wear in Controlling the Progression of Childhood Myopia

NCT04806698 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2021-03-19

No results posted yet for this study

Summary

To assess the long-term efficacy of the Menicon Z Night orthokeratology contact lens in controlling the progression of childhood myopia

Conditions

  • Myopia, Progressive
  • Children, Only

Interventions

DEVICE

Menicon Z Night

Children wearing Menicon Z Night orthokeratology contact lenses

DEVICE

Control

Children wearing distance single-vision glasses or distance single-vision soft contact lenses

Sponsors & Collaborators

  • Menicon Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2007-03-01
Primary Completion
2015-03-01
Completion
2015-03-01

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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 NCT04806698 on ClinicalTrials.gov