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Clinical Comparison of Silicone Hydrogel and HEMA-based Daily Disposable Contact Lenses

NCT01362907 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2012-08-03

Study results available
· View outcomes & findings →

Summary

The purpose of this trial was to compare the performance of an investigational daily disposable contact lens to a commercially available daily disposable contact lens.

Conditions

  • Myopia

Interventions

DEVICE

Delefilcon A contact lens

Investigational, silicone hydrogel, single vision, soft contact lens for daily disposable wear

DEVICE

Etafilcon A contact lens

Commercially marketed, HEMA-based, single vision, soft contact lens for daily disposable wear

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2011-06-30
Completion
2011-06-30

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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 NCT01362907 on ClinicalTrials.gov