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A Clinical Comparison of Two Daily Disposable Soft Contact Lenses

NCT04005885 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 55

Last updated 2021-01-05

Study results available
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Summary

This double-masked, randomized, bilateral, crossover, direct refit study compared the clinical performance of two daily disposable contact lenses (somofilcon A and stenfilcon A) when fitted to existing wearers of comfilcon A monthly lenses.

Conditions

  • Myopia

Interventions

DEVICE

comfilcon A

Contact Lens

DEVICE

somofilcon A

daily disposable contact lens

DEVICE

stenfilcon A

daily disposable contact lens

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Carole Maldonado-Codina, PhD, MCOptom, FAAO, FBCLA · Eurolens Research

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2019-03-01
Primary Completion
2019-11-08
Completion
2019-11-30
FDA Device
Yes

Countries

  • United Kingdom

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 NCT04005885 on ClinicalTrials.gov