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Clinical Comparison of Two Daily Disposable Silicone Hydrogel Soft Contact Lens

NCT02676258 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2016-07-07

No results posted yet for this study

Summary

The objective of this study is to evaluate a new daily disposable silicone hydrogel soft contact lens by comparing to an existing daily disposable soft contact lens.

Conditions

  • Myopia

Interventions

DEVICE

Si-Hy (olifilcon B)

Wear Si-Hy silicone hydrgel soft contact lens for 3 months

DEVICE

Vistakon (narafilcon A)

Wear Vistakon soft contact lens for 3 months

Sponsors & Collaborators

  • Visco Vision Inc.

    lead INDUSTRY

Principal Investigators

  • Huey Chuan Cheng, MD MS · Mackay Memorial Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2015-11-30
Completion
2015-11-30

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 NCT02676258 on ClinicalTrials.gov