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A Clinical Study Comparing the Comfort of Three Commercially Available Contact Lenses

NCT02298400 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2024-04-25

No results posted yet for this study

Summary

The purpose of this study is to compare the comfort of three commercially available contact lenses.

Conditions

  • Contact Lens Complication

Interventions

DEVICE

Acuvue® Oasys® Lenses (senofilcon A)

Contact lenses placed in each eye during the day for about 8 hours

DEVICE

30-Day Bausch + Lomb PureVision (balafilcon A)

Contact lenses placed in each eye during the day for about 8 hours

DEVICE

Clariti® 1-Day (Somofilcon A)

Contact lenses placed in each eye during the day for about 8 hours

Sponsors & Collaborators

  • ORA, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-08-31
Primary Completion
2014-09-30
Completion
2014-09-30

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 NCT02298400 on ClinicalTrials.gov