Status:

COMPLETED

Multi-Center Clinical Evaluation of Two Daily Disposable Contact Lenses

Lead Sponsor:

Alcon Research

Conditions:

Myopia

Refractive Error

Eligibility:

All Genders

18-45 years

Phase:

NA

Brief Summary

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

Eligibility Criteria

Inclusion

  • Adapted soft contact lens wearer;
  • Spherical distance contact lens prescription between -1.00 and -6.00 diopter (inclusive);
  • Spectacle cylinder ≤0.75 diopter in the least astigmatic eye, ≤1.00 diopter in the other;
  • Correctable to 6/9 (20/30) in both eyes;
  • Read, understood and signed the informed consent;
  • Willing to comply with the wear schedule;
  • Willing to comply with the study visit schedule;
  • Other protocol-defined inclusion criteria may apply.

Exclusion

  • Any active corneal infection, injury or inflammation;
  • Systemic or ocular allergies which might interfere with contact lens wear;
  • Systemic or ocular disease which might interfere with contact lens wear;
  • Strabismus or amblyopia;
  • Corneal refractive surgery and any anterior segment surgery;
  • Use of systemic/topical medication contraindicating contact lens wear;
  • Use of gas permeable contact lenses within 1 month preceding the study;
  • Participation in any concurrent clinical trial or in the last 30 days;
  • Other protocol-defined exclusion criteria may apply.

Key Trial Info

Start Date :

August 1 2013

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2013

Estimated Enrollment :

89 Patients enrolled

Trial Details

Trial ID

NCT01898260

Start Date

August 1 2013

End Date

October 1 2013

Last Update

May 12 2015

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Alcon Investigative Site

Surrey, United Kingdom