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Clinical Trial Summary

The aim of this study is to assess the visual performance of prototype soft contact lens designs compared to a commercially available contact lens


Clinical Trial Description

Prospective, participant-masked, randomised, stratified, crossover, bilateral wear, dispensing clinical trial where participants will wear the prototype (test) and the commercial (control) lens. A minimum of an overnight washout period is required between the fitting /assessment visits. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject)


Related Conditions & MeSH terms


NCT number NCT02193555
Study type Interventional
Source Brien Holden Vision
Contact
Status Completed
Phase N/A
Start date July 2014
Completion date November 2014

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