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Comparative Study of Two Marketed 1-day Soft Contact Lenses

NCT01464255 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 71

Last updated 2014-08-19

Study results available
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Summary

This study is designed to evaluate ocufilcon D lens compared to ocufilcon B lens in a 1-week crossover, daily wear regimen.

Conditions

  • Myopia

Interventions

DEVICE

ocufilcon D

Participants wear a first pair of lenses for one week and then crossover and wear an alternate second pair of lenses for one week.

DEVICE

ocufilcon B

Participants wear a first pair of lenses for one week and then crossover and wear an alternate second pair of lenses for one week.

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Thao N Yeh, OD · U.C. Berkeley, School of Optometry

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Primary Completion
2011-10-31
Completion
2011-11-30

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 NCT01464255 on ClinicalTrials.gov