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Clinical Comparison of 4 Daily Disposable Soft Contact Lenses

NCT03349632 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 68

Last updated 2019-02-22

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to obtain on-eye performance data to inform contact lens product development and to further evaluate product performance in the intended population.

Conditions

  • Refractive Error

Interventions

DEVICE

verofilcon A contact lenses

Investigational spherical silicone hydrogel contact lenses for daily disposable wear

DEVICE

senofilcon A contact lenses

Commercially available spherical silicone hydrogel contact lenses for daily disposable wear

DEVICE

stenfilcon A contact lenses

Commercially available spherical silicone hydrogel contact lenses for daily disposable wear

DEVICE

etafilcon A contact lenses

Commercially available spherical silicone hydrogel contact lenses for daily disposable wear

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-10
Primary Completion
2018-02-16
Completion
2018-02-16
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 NCT03349632 on ClinicalTrials.gov