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Daily Disposable Comparison Study

NCT02094677 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2020-07-28

Study results available
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Summary

The objective of the study is to compare the overall subjective preference between two Daily Disposable hydrogel lenses when refitted into a third hydrogel lens.

Conditions

  • Myopia

Interventions

DEVICE

filcon II 3

Participants were randomized to wear filcon II 3 test lens.

DEVICE

etafilcon A

Participants were randomized to wear etafilcon A control lens.

DEVICE

nelfilcon A

Participants were randomized to wear nelfilcon A control lens.

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2014-03-31
Primary Completion
2014-04-30
Completion
2014-04-30

Countries

  • Canada

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 NCT02094677 on ClinicalTrials.gov