Clinical Evaluation of Investigational Multifocal Toric Contact Lenses
- Conditions
- PresbyopiaAstigmatism
- Interventions
- Device: comfilcon A multifocal toric lensDevice: omafilcon A Multifocal Toric Lens
- Registration Number
- NCT03519282
- Lead Sponsor
- Coopervision, Inc.
- Brief Summary
This non-dispensing study is to evaluate the clinical performance of a test multifocal toric silicone hydrogel contact lens compared to a marketed multifocal toric contact lens (control).
- Detailed Description
This non-dispensing study is to evaluate the clinical performance of a test multifocal toric silicone hydrogel contact lens compared to a marketed multifocal toric contact lens (control).
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 13
- Has had a self-reported oculo-visual examination in the last two years.
- Is aged 40-75 years, inclusive and has full legal capacity to volunteer.
- Has read and understood the participant information sheet.
- Is willing and able to follow instructions and maintain the appointment schedule.
- Is able to participate in Parts A and B related to this work.
- Has a contact lens spherical prescription between +10.00 to -10.00D (inclusive).
- Has an Add component to their spectacle refraction (between +0.75 and +2.50DS).
- Has astigmatism between -0.75 and -5.75DC (based on the vertexed ocular refraction in each eye.
- Can be satisfactorily fitted with the study lenses.
- Is correctable to a visual acuity of 20/40 (0.30 logMAR) or better (in each eye) with their habitual vision correction or 20/25 (0.10 logMAR) best-corrected.
- They have successfully worn soft contact lenses in the last six months
- Has clear corneas and no active ocular disease.
- Has not worn lenses for at least 12 hours before the examination.
- Has an up-to-date pair of spectacles.
- Has never worn contact lenses before.
- Has any systemic disease affecting ocular health.
- Is using any systemic or topical medications that will affect ocular health.
- Has any ocular pathology or severe insufficiency of lacrimal secretion (moderate to severe dry eyes) that would, in the opinion of the investigator, affect the wearing of contact lenses.
- Has persistent, clinically significant corneal or conjunctival staining using sodium fluorescein dye that would, in the opinion of the investigator, be problematic for their participation in the study.
- Has any clinically significant lid or conjunctival abnormalities, active neovascularization or any central corneal scars.
- Is aphakic.
- Has undergone corneal refractive surgery.
- Has a history of anaphylaxis or severe allergic reaction.
- Has diabetes or an infectious or immunosuppressive disease which could contraindicate contact lens wear or pose a risk to the investigator.
- They are pregnant or breast-feeding.
- Is participating in any other type of eye-related clinical or research study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Test Multifocal Toric Lens comfilcon A multifocal toric lens comfilcon A multifocal toric lens Test Multifocal Toric Lens omafilcon A Multifocal Toric Lens comfilcon A multifocal toric lens omafilcon A Multifocal Toric Lens comfilcon A multifocal toric lens Control multifocal toric lens omafilcon A Multifocal Toric Lens omafilcon A Multifocal Toric Lens Control multifocal toric lens
- Primary Outcome Measures
Name Time Method Visual Acuity Up to 2 hours Visual Acuity (measured in LogMAR)
- Secondary Outcome Measures
Name Time Method Assessment of Visual Performance: Intermediate Task for Vision Quality and Clarity Up to 2 hours Subjective assessment of visual performance for intermediate task for vision quality and clarity was assessed on a scale 0-100, 0=poor, 100=excellent.
Assessment of Visual Performance: Distance Navigation Tasks for Vision Quality and Clarity Up to 2 hours Subjective assessment of visual performance for distance navigation tasks for vision quality and clarity was assessed on a scale 0-100, 0=poor, 100=excellent.
Assessment of Visual Performance: Near Task for Vision Quality and Clarity Up to 2 hours Subjective assessment of visual performance for near task for vision quality and clarity was assessed on a scale 0-100, 0=poor, 100=excellent.
Trial Locations
- Locations (1)
Eurolens Research
🇬🇧Manchester, United Kingdom