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Comparative Study of Two Marketed Spherical Soft Contact Lenses

NCT01582789 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 61

Last updated 2020-10-27

Study results available
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Summary

The purpose of this study is to obtain objective and subjective clinical data to compare the performance of two soft contact lenses.

Conditions

  • Refractive Error

Interventions

DEVICE

enfilcon A

enfilcon A daily wear soft contact lens

DEVICE

senofilcon A

senofilcon A daily wear soft contact lens

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Don Siegel, OD · CooperVision, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
38 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-04-09
Primary Completion
2012-05-31
Completion
2012-07-31
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 NCT01582789 on ClinicalTrials.gov