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

NCT06716372 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 134

Last updated 2025-10-02

No results posted yet for this study

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

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.

Sponsors & Collaborators

  • Visco Vision Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-07
Primary Completion
2025-08-20
Completion
2025-08-20

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06716372 on ClinicalTrials.gov