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DAILIES TOTAL1® - Comparative Assessment of Tear Film Evaporation

NCT02517567 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 37

Last updated 2018-07-02

Study results available
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Summary

The purpose of this study is to evaluate the tear film evaporation of symptomatic soft contact lens wearers in the absence of contact lens wear and after at least 8 hours of contact lens wear.

Conditions

  • Refractive Error

Interventions

DEVICE

Delefilcon A contact lenses

Daily disposable, silicone hydrogel contact lenses used according to manufacturer's instructions

DEVICE

Narafilcon A contact lenses

Daily disposable, silicone hydrogel contact lenses used according to manufacturer's instructions

DEVICE

Somofilcon A contact lenses

Daily disposable, silicone hydrogel contact lenses used according to manufacturer's instructions

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Clinical Manager, Clinical Trial Management · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-21
Primary Completion
2016-04-22
Completion
2016-04-22

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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 NCT02517567 on ClinicalTrials.gov