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Clinical Evaluation of Two Daily Disposable Contact Lenses

NCT01875471 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 279

Last updated 2018-06-19

Study results available
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Summary

The objective of this study is to compare the ease of removing two daily disposable soft contact lenses off the eye.

Conditions

  • Refractive Error

Interventions

DEVICE

delefilcon A

Daily disposable soft contact lens to be worn at least 8 hours daily

DEVICE

narafilcon A

Daily disposable contact lens to be worn at least 8 hours daily

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2013-06-30
Primary Completion
2013-08-31
Completion
2013-08-31

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 NCT01875471 on ClinicalTrials.gov