Clinical Comparison of Two Daily Disposable Lenses Among Daily Disposable Lens Wearers | NCT01134211 | Trialant
CompletedInterventionalNot ApplicableUpdated Nov 21, 2016
Clinical Comparison of Two Daily Disposable Lenses Among Daily Disposable Lens Wearers
ClinicalTrials.gov ID
NCT01134211
Lead Sponsor
CIBA VISIONINDUSTRY
Overall Status
Completed
Study Type
Interventional
Phase
Not Applicable
Enrollment
316Actual
Last Update Posted
Nov 21, 2016Estimated
Start Date
May 2010
Primary Completion Date
Jul 2010Actual
Completion Date
Jul 2010Actual
Brief Summary
The primary objective of this trial is to evaluate the subjective performance of two different daily disposable contact lenses in a population of daily disposable lens wearers.
Myopia
nelfilcon A
filcon II 3
Ages Eligible for Study
Child (0-17)Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Currently wearing any spherical daily disposable lens in daily wear, daily disposable modality for at least 3 months prior to enrollment with the exception of the 2 study products
Currently Wearing lenses at least 8 hrs/day and 5 days/week.
Other protocol-defined inclusion criteria may apply.
Exclusion Criteria:
Eye injury or surgery within twelve weeks immediately prior to enrollment for this trial.
Pre-existing ocular irritation that would preclude contact lens fitting.
Currently enrolled in any clinical trial.
Evidence of systemic or ocular abnormality, infection, or disease which is likely to affect successful wear of contact lenses or use of their accessory solutions as determined by the investigator.
Any use of medications for which contact lens wear could be contraindicated as determined by the investigator.
Prior history of corneal or refractive surgery.
Requires monovision correction.
Other protocol-defined exclusion criteria may apply.