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Clinical Trial Summary

The purpose of this study is to evaluate the clinical performance of two daily disposable silicone hydrogel contact lenses. One of these lenses, the 'test' lens is an investigational product. This means that it has not yet been approved for commercial use and is not available for sale. The other lens (control) is a commercially available contact lens.

The results of this study will be analysed to determine how the 'test' lens compares with the 'control' lens. The control lens has been chosen because it is a market leader and is well tried and tested.

Participants who are in this study will need to have healthy eyes, except for the need to correct their eyesight. Up to 90 people who are aged 20 years or older will be considered for participation in this study. The study is designed to be approximately 3 months long.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03859440
Study type Interventional
Source HOYA Lamphun Ltd
Contact Atsushi Uchida
Phone +81 3 5913 2378
Email atsushi.uchida@hoya.com
Status Not yet recruiting
Phase N/A
Start date May 2019
Completion date October 2019

See also
  Status Clinical Trial Phase
Active, not recruiting NCT05433259 - Biometric Factors Changes Caused by Myopia Orthokeratology (OK) Lens N/A
Completed NCT00940459 - Subjective and Conjunctival Response to Edge Design of Different Silicone Hydrogels N/A
Completed NCT02921087 - Connecting Contact Lenses and Digital Technology N/A
Completed NCT01192126 - A Study to Evaluate the Product Performance of a Daily Disposable Contact Lens N/A
Completed NCT00982046 - A Clinical Comparison of Three Contact Lens Care Systems and Their Effect on Contact Lenses N/A