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Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses

NCT05431478 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 68

Last updated 2023-09-21

Study results available
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Summary

The purpose of this study is to assess the clinical performance of two reusable silicone hydrogel contact lenses when worn on a daily wear basis.

Conditions

  • Refractive Errors

Interventions

DEVICE

Serafilcon A contact lenses

Reusable silicone hydrogel contact lenses worn during the day and removed at night for daily cleaning and disinfection

DEVICE

Senofilcon A contact lenses

Reusable silicone hydrogel contact lenses worn during the day and removed at night for daily cleaning and disinfection

DEVICE

CLEAR CARE

Hydrogen peroxide based contact lens cleaning and disinfecting solution

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Clinical Trial Lead, CDMA Vision Care · Alcon Research, LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-15
Primary Completion
2022-09-09
Completion
2022-09-09
FDA Device
Yes

Countries

  • United States

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 NCT05431478 on ClinicalTrials.gov