Myopia Clinical Trial - Euclid Phoenix Lens Design Trial 2

Status Not yet recruiting

Clinical Trial Summary

Lens wettability and subjective comfort of Euclid orthokeratology lenses with and without an enhanced coating will be compared in 50 children. Axial elongation will be monitored in pediatric patients who qualify and consent.

Clinical Trial Description

The primary objective of this trial is to provide an assessment of the lens wettability and patient comfort with an enhanced surface treatment for the Emerald Lens design when used by practitioners with moderate experience with fitting Euclid orthokeratology lenses. The hypothesis to be tested is that the proportion of participants with a lens wettability score of > 3 (on a 5 point scale) with the enhanced surface treatment will be greater than that of the current lens surface, using a 1 to 5 scale The primary outcome variable is lens wettability as measured on eye using a 1 to 5 scale This clinical investigation will be a prospective, randomized, double-masked two-arm non-crossover trial. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06392607
Study type	Interventional
Source	Euclid Systems Corporation
Contact	Sally Dillehay, OD, EdD
Phone	7705214358?
Email	sally.dillehay@clintrialsolutions.org
Status	Not yet recruiting
Phase	N/A
Start date	May 2024
Completion date	September 2025

View Details

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