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Evaluation Of One Silicone Hydrogel Contact Lens and Two Hydrogel Lenses in Daily Wear

NCT04050618 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 114

Last updated 2020-10-19

Study results available
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Summary

To evaluate the comparative clinical performance of the fanfilcon A silicone hydrogel lens used in daily wear and to compare this with competitive hydrogel lens products.

Conditions

  • Myopia

Interventions

DEVICE

fanfilcon A test lens

Silicone hydrogel contact lens

DEVICE

ocufilcon D control lens

hydrogel contact lens

DEVICE

etafilcon A control lens

hydrogel contact lens

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • David C Ardaya, OD · Golden Optometric Group

  • William J Bogus, OD · Office of William J. Bogus, O.D.

  • Bryan E Frazier, OD · Frazier Vision, Inc

  • Wayne Golden, OD · Golden Vision

  • Andrew J Sacco, OD · Sacco Eye Group

  • Christopher Pearson, OD · Omega Vision Center PA (DBA Sabal Eye Care)

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-09
Primary Completion
2019-09-24
Completion
2019-11-08
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 NCT04050618 on ClinicalTrials.gov