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Clinical Evaluation of ACUVUE® OASYS® 1-Day and ACUVUE® OASYS®

NCT02696317 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 84

Last updated 2018-07-02

Study results available
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Summary

The purpose of this study is to evaluate the performance of two commercially-available silicone hydrogel contact lenses in normal and low humidity environments after at least 7 days of wear.

Conditions

  • Refractive Error

Interventions

DEVICE

Senofilcon A contact lenses with HydraLuxe™

Contact lenses worn during Period 1 or 2, as randomized

DEVICE

Senofilcon A contact lenses

Contact lenses worn during Period 1 or 2, as randomized

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Senior Clinical Manager, GCRA Operations · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-18
Primary Completion
2016-06-06
Completion
2016-06-06

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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 NCT02696317 on ClinicalTrials.gov