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Dehydration of Stenfilcon A Contact Lenses Versus Delefilcon A Contact Lenses

NCT02366923 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2020-07-29

Study results available
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Summary

The study will explore in vivo lens dehydration rates across a 12hr wear period for the study lenses.

Conditions

  • Myopia

Interventions

DEVICE

stenfilcon A

Each subject randomized to wear either the test or control in either the left of right eye.

DEVICE

delefilcon A

Each subject randomized to wear either the test or control in either the left of right eye.

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Lydon Jones, PhD FC · Director, Centre for Contact Lens Research

  • Farah Panjwani, BSc RAQ · Univerisy of Waterloo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2015-04-30
Completion
2015-06-30

Countries

  • Canada

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 NCT02366923 on ClinicalTrials.gov