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

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Phase 3
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 7
Maximum Age: 11
Healthy Volunteers: f
View:

• Spherical refractive error between -1.00D and -4.50D

• Astigmatism of ≤1.00D

• No history of orthokeratology or atropine use

• No ocular diseases or surgical history

Locations
Other Locations
New Zealand
Auckland Myopia Clinic
RECRUITING
Auckland
Contact Information
Primary
James S Wolffsohn, BSc PhD DSc
j.s.w.wolffsohn@aston.ac.uk
+447833049245
Backup
Vivienne Wang, BSc
210269613@aston.ac.uk
Time Frame
Start Date: 2026-03-21
Estimated Completion Date: 2026-12-30
Participants
Target number of participants: 66
Treatments
Active_comparator: MiSight Contact Lens
Commercially available myopia control contact lens
Active_comparator: Abiliti 1-Day
Commercially available myopia control contact lens
Related Therapeutic Areas
Sponsors
Leads: Aston University

This content was sourced from clinicaltrials.gov