NCT06716372

A Clinical Trial to Evaluate the Vision Correction Safety and Efficacy of DSiHy Silicone Hydrogel Soft Contact Lens

A Prospective, Randomized, Double-blind, Parallel, Active-controlled Clinical Trial to Evaluate the Vision Correction Safety and Efficacy of DSiHy Silicone Hydrogel Soft Contact Lens

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 134 (actual)
• Sponsor: Visco Vision Inc. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This is a prospective, randomized, double-blind, parallel, active-controlled, multi-center clinical study. The purpose is to evaluate the safety and effectiveness wearing "DSiHy Silicone Hydrogel Soft Contact Lens". Subjects will be randomized in 1:1 ratio to wear either the investigational device "DSiHy Silicone Hydrogel Soft Contact Lens" or the control device Daily Silicone Hydrogel Contact Lenses(oB)".

Conditions

• Myopia
• Refractive Errors

Interventions

Type	Name	Description
DEVICE	DSiHy Silicone Hydrogel Soft Contact Lens	The daily wear, daily disposable soft contact lens for the correction of myopia and hyperopia in person with non-diseased eyes.
DEVICE	Daily Silicone Hydrogel Contact Lenses (oB)	The daily wear, daily disposable soft contact lens for the correction of myopia and hyperopia in person with non-diseased eyes.

Timeline

• Start date: 2024-10-07
• Primary completion: 2025-08-20
• Completion: 2025-08-20
• First posted: 2024-12-04
• Last updated: 2025-10-02

Locations

3 sites across 1 country: Taiwan