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Multi-Center Clinical Evaluation of Two Daily Disposable Contact Lenses

NCT01898260 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 89

Last updated 2015-05-12

No results posted yet for this study

Summary

The purpose of this study is to compare the subjective performance of two daily disposable contact lenses with respect to comfort and handling.

Conditions

  • Myopia
  • Refractive Error

Interventions

DEVICE

Ultrafilcon B contact lens

Silicone hydrogel contact lens CE-marked for daily disposable wear. Private-label versions may be used.

DEVICE

Stenfilcon A contact lens

Silicone hydrogel contact lens CE-marked for daily disposable wear. Private-label versions may be used.

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Joachim Nick, Dipl. Ing. · Alcon Research

Study Design

Allocation
RANDOMIZED
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-08-31
Primary Completion
2013-10-31
Completion
2013-10-31

Countries

  • United Kingdom

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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 NCT01898260 on ClinicalTrials.gov