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Discontinuation of Lens Wear in New Ortho-k Children (DOEE2)

NCT01236755 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 91

Last updated 2020-03-11

Study results available
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Summary

This study aims at investigating the efficacy of myopic control using ortho-k in younger and older children.

Conditions

  • Myopia

Interventions

DEVICE

single-vision glasses

Daily wear of glasses to correct vision in the first seven months of the study

DEVICE

ortho-k lenses

Nightly wear of lenses to correct vision in day time in the second seven months of the study

Sponsors & Collaborators

  • Menicon Co., Ltd.

    collaborator INDUSTRY

  • The Hong Kong Polytechnic University

    lead OTHER

Principal Investigators

  • Pauline Cho, PhD · The Hong Kong Polytechnic University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2010-10-31
Primary Completion
2013-07-31
Completion
2013-12-31

Countries

  • China

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 NCT01236755 on ClinicalTrials.gov