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Clinical Evaluation of Stenfilcon A Soft Contact Lens When Compared to Ocufilcon B Soft Contact Lens

NCT01354223 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2020-07-29

Study results available
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Summary

This study seeks to evaluate a new daily disposable contact lens compared to an existing daily disposable contact lens.

Conditions

  • Myopia

Interventions

DEVICE

stenfilcon A contact lens

Randomized to stenfilcon A contact lens worn in a daily wear, daily disposable mode

DEVICE

ocufilcon B contact lens

Daily disposable contact lens worn in a daily wear, daily disposable mode

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Stephen Byrnes, OD

  • Lee Rigel, OD

  • Mary Jo Stiegemeier, OD

  • Peter Van Hoven, OD

  • Eric White, OD

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-10-31
Primary Completion
2011-03-31
Completion
2011-04-30

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 NCT01354223 on ClinicalTrials.gov