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Clinical Trials/NCT02815735
NCT02815735
Completed
Not Applicable

Multi-Centre Clinical Evaluation of Two Reusable Soft Contact Lenses

Coopervision, Inc.9 sites in 1 country85 target enrollmentAugust 2016
ConditionsMyopia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myopia
Sponsor
Coopervision, Inc.
Enrollment
85
Locations
9
Primary Endpoint
Comfort During the Day
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The aim of this study is to compare the subjective performance of the comfilcon A contact lens against lotrafilcon B contact lens after 4 weeks of reusable lens wear.

Detailed Description

This will be a 80 subject, randomized, bilateral, double-masked, dispensing, cross-over study comparing comfilcon A versus lotrafilcon B lenses over 4 weeks of daily wear for each lens pair.

Registry
clinicaltrials.gov
Start Date
August 2016
End Date
February 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Spherical distance CL (Contact Lens) prescription between -1.00 and -6.00D (Diopter) OR in both eyes (inclusive)
  • Adapted soft CL wearers (i.e. \>1 month) who are reusable lens wearers\*
  • Spectacle cylinder 0.75D in both eyes
  • Correctable to 6/9 in both eyes
  • Be between 18 and 34 years of age (inclusive)
  • Able to read, comprehend and sign an informed consent
  • Own a mobile phone and be able to respond to SMS survey during the period 8am - 8pm
  • Willing to comply with the wear and study visit schedule

Exclusion Criteria

  • Any of the following will render a subject ineligible for inclusion:
  • Existing wearer of daily disposable contact lenses
  • Known allergy to Opti-Free PureMoist multipurpose solution
  • Any active corneal infection, injury or inflammation
  • Systemic or ocular allergies, which might interfere with CL wear
  • Systemic disease, which might interfere with CL wear
  • Ocular disease, which might interfere with CL wear
  • Strabismus or amblyopia
  • Subjects who have undergone corneal refractive surgery
  • Subjects with keratoconus or other severe corneal irregularity contraindicating lens wear

Outcomes

Primary Outcomes

Comfort During the Day

Time Frame: Days 3, 12, 26

Comfort during the day for comfilcon A and lotrafilcon B lenses assessed via via SMS (short message service) text message at days 3,12, and 26 at hours 8:00 am, 12:00 pm, 4:00 pm, and 8:00 pm. Scale 0-10, 0=painful, 10=can't feel the lenses.

Comfort

Time Frame: Baseline, 2 weeks, 4 weeks

Comfort (insertion, end of the day, and overall) for habitual lenses assessed at baseline and comfilcon A and lotrafilcon B lenses assessed at 2 weeks and 4 weeks. Scale 0-10, 0=painful, 10=can't feel the lenses.

Study Sites (9)

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