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Daily Disposable Contact Lens Tear Film Study

NCT01473160 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2013-04-17

Study results available
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Summary

The purpose of this study was to evaluate the pre-lens tear film stability of a new CE-marked daily disposable contact lens as compared to a commercially available daily disposable contact lens.

Conditions

  • Myopia

Interventions

DEVICE

delefilcon A contact lens

CE-marked, silicone hydrogel, single vision, soft contact lens for daily disposable wear

DEVICE

narafilcon A contact lens

Commercially marketed, silicone hydrogel, single vision, soft contact lens for daily disposable wear.

Sponsors & Collaborators

  • Aston University

    collaborator OTHER

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2011-12-31
Completion
2011-12-31

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 NCT01473160 on ClinicalTrials.gov