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Clinical Trial Summary

To compare the rate of myopia progression of contact lenses utilising S.T.O.P.® technology against MiSight® contact lenses.


Clinical Trial Description

Myopic children (8-14 years of age) will be randomly allocated to wear one of 3 contact lens options (MiSight®, S.T.O.P.®- F2 or S.T.O.P.®- DT) bilaterally on a daily wear basis. The overall trial duration, including follow-up period, is expected to be approximately 48 months. Each participant's duration is expected to be approximately 36 months. The visits are Baseline / Fit, Dispensing, 1 week, 1 month, 6 months then visits every 6 months after. All procedures performed at these visits are standard, non invasive clinical tests. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05243836
Study type Interventional
Source nthalmic Pty Ltd
Contact Daniel Tilia, MOptom, PhD
Phone +61290377700
Email d.tilia@nthalmic.com
Status Recruiting
Phase N/A
Start date August 4, 2023
Completion date January 2028

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