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The Effect of Myopia-Control Contact Lenses in New Zealand Chinese Children

NCT07535749 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2026-04-17

No results posted yet for this study

Summary

The study will employ a randomized, controlled, investigator-masked paired-eye comparison design to evaluate the effects of two myopia-control contact lenses-MiSight 1 Day and Abiliti 1-Day-in New Zealand Chinese children.

The study duration will be 6 months, with assessments conducted at baseline, 2 weeks, 3 months, and 6 months.

The clinical research will be conducted at the Auckland Myopia Clinic (New Zealand) and will follow a standard clinical routine for children with early myopia, the only difference being the randomizing of the MiSight and Abiliti contact lenses between the two eyes of the participants.

Conditions

  • Myopia Progression

Interventions

DEVICE

MiSight Contact Lenses (CooperVision)

Myopia Control Contact Lens

DEVICE

Albiliti 1-Day (Johnson and Johnson, VisionCare)

Myopia Control Contact Lens

Sponsors & Collaborators

  • Aston University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
7 Years
Max Age
11 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-21
Primary Completion
2026-11-30
Completion
2026-12-30

Countries

  • New Zealand

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 NCT07535749 on ClinicalTrials.gov