Assessment of an Investigational Frequent Replacement Silicone Hydrogel Lens
Refractive Ametropia
About this trial
This is an interventional treatment trial for Refractive Ametropia
Eligibility Criteria
Inclusion Criteria: Able to understand and sign an Informed Consent Form. Willing to attend all scheduled study visits as required per protocol. Willing and able to wear assigned study lenses as required per protocol. Successful wear of spherical daily wear or extended wear frequent replacement soft contact lenses in both eyes during the past 3 months for a minimum of 5 days per week. Manifest cylinder ≤ 0.75 diopter (D) in each eye. Other protocol-specified inclusion criteria may apply. Exclusion Criteria: Any eye infection, inflammation, or abnormality or disease (including systemic) that contraindicates contact lens wear, as determined by the Investigator. Any use of systemic or ocular medications for which contact lens wear could be contraindicated, as determined by the Investigator. History of eye surgery, including refractive surgery. Currently pregnant or breast-feeding. Monovision contact lens wearers. Daily disposable contact lens wearers. Other protocol-specified exclusion criteria may apply.
Sites / Locations
- Family EyeCare Center
- Winston Eye Care
- Kurata Eye Care Center
- East West Eye Institute
- Dr.Elsa Pao, O.D
- Gordon Schanzlin New Vision Institute
- Complete Family Vision Care
- Westview Optometry
- OMEGA Vision Center PA, DBA Sabal Eye Care
- Kindred Optics at Maitland Vision Center
- Mid Florida Eye Center, PA
- Eola Eyes
- Vision Health Institute
- Visual Performance Center Research & Development
- Golden Vision
- Advanced Eyecare Specialists
- VisionPoint Eye Center
- Franklin Park Eye Center, PC
- Kannarr Eye Care, LLC
- Optimum Vision Care
- Fraser Eye Care Center
- Dr. Schwartz Optometrist and Associates
- Complete Eye Care of Medina
- Fischer Laser Eye Center, LLC
- Tekwnai Vision Center, Inc
- Alterman, Modi & Wolter
- Rochester Ophthalmological Group, PC
- Asheville Eye Associates, PLLC
- ProCare Vision Centers, Inc.
- Midwest Vision Care
- EyeCare Professionals, Inc. DBA Insight Research Clinic, LLC
- Wyomissing Optometric Center
- West Bay Eye Associates
- North Spartanburg Eye Center
- Primary Eyecare Group, PC
- Optometry Group, PLLC
- Total Eye Care, PA
- Advancing Vision Research, LLC
- Beaumont Family Eye Care
- Vision One Eyecare
- Dawn M Rakich, OD
- Clarke EyeCare Center
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
LID015385
Biofinity
LID015385 soft contact lenses worn in both eyes for up to 6 nights/7 days continuously (awake and asleep). Must sleep 1 night per week without lenses. Lenses will be replaced as specified in the study protocol.
Comfilcon A soft contact lenses worn in both eyes for up to 6 nights/7 days continuously (awake and asleep). Must sleep 1 night per week without lenses. Lenses will be replaced as specified in the study protocol.