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Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear

NCT03095027 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2019-02-04

Study results available
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Summary

The purpose of this study is to compare the visual acuity of an investigational silicone hydrogel to a commercially available silicone hydrogel in contact lens wearers.

Conditions

  • Refractive Error

Interventions

DEVICE

FID122819 contact lenses

Investigational 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

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Sr. Clinical Manager, Trial Management Operations · Alcon, A Novartis Division

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-04-19
Primary Completion
2017-05-15
Completion
2017-05-15
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 NCT03095027 on ClinicalTrials.gov