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Myopia Control With Orthokeratology Contact Lenses in Spain

NCT04806763 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 69

Last updated 2021-03-26

No results posted yet for this study

Summary

The purpose of this prospective study is to assess the efficacy, safety and patient-reported outcomes of the Menicon Z Night orthokeratolgy contact lens for reducing myopia progression in children.

Conditions

  • Myopia, Progressive
  • Children, Only
  • Contact Lens Complication
  • Perception, Self
  • Axial Myopia

Interventions

DEVICE

Menicon Z Night

To assess the use of Menicon Z Night contact lenses for reducing myopia progression in children

DEVICE

Control

Distance, single-vision glasses were used as control

Sponsors & Collaborators

  • Universidad Europea de Madrid

    collaborator OTHER

  • Aston University

    collaborator OTHER

  • Clinica novovision

    collaborator UNKNOWN

  • 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
2010-03-01
Completion
2010-03-01

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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 NCT04806763 on ClinicalTrials.gov