Performance of Toric Silicone Hydrogel Contact Lenses Following One Month of Daily Wear
- Conditions
- Astigmatism
- Interventions
- Device: Fanfilcon A toric lensDevice: Lotrafilcon B toric lens
- Registration Number
- NCT03418064
- Lead Sponsor
- Coopervision, Inc.
- Brief Summary
The aim of this prospective study is to evaluate the clinical performance of fanfilcon A toric and lotrafilcon B toric contact lenses after 1 month of wear in each pair.
- Detailed Description
The aim of this prospective study is to evaluate the clinical performance of Avaira Vitality toric (fanfilcon A) and AIR OPTIX for Astigmatism (lotrafilcon B) contact lenses after 1 month of wear in each pair.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 42
- Is between 18 and 40 years of age (inclusive)
- Has had a self-reported visual exam in the last two years
- Is an adapted soft contact lens wearer
- Has a contact lens spherical prescription between +6.00 to - 9.00 (inclusive)
- Have no less than -0.75D of astigmatism and no more than -2.25 D in both eyes.
- Can achieve best corrected spectacle distance visual acuity of 20/25 (0.10 logMAR) or better in each eye.
- Can achieve a distance visual acuity of 20/30 (0.18 logMAR) or better in each eye with the study contact lenses.
- Has clear corneas and no active ocular disease
- Has read, understood and signed the information consent letter.
- Patient contact lens refraction should fit within the available parameters of the study lenses.
- Is willing to comply with the wear schedule (at least 5 days per week, > 8 hours/day assuming there are no contraindications for doing so).
- Is willing to comply with the visit schedule
A person will be excluded from the study if he/she:
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Has a CL prescription outside the range of the available parameters of the study lenses.
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Has a spectacle cylinder less than -0.75D or more than -2.50 D of cylinder in either eye.
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Has a history of not achieving comfortable CL wear (5 days per week; > 8 hours/day)
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Has contact lens best corrected distance vision worse than 20/25 (0.10 logMAR) in either eye.
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Presence of clinically significant (grade 2-4) anterior segment abnormalities
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Presence of ocular or systemic disease or need of medications which might interfere with contact lens wear.
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Slit lamp findings that would contraindicate contact lens wear such as:
- Pathological dry eye or associated findings
- Pterygium, pinguecula, or corneal scars within the visual axis
- Neovascularization > 0.75 mm in from of the limbus
- Giant papillary conjunctivitis (GCP) worse than grade 1
- Anterior uveitis or iritis (past or present)
- Seborrheic eczema, Seborrheic conjunctivitis
- History of corneal ulcers or fungal infections
- Poor personal hygiene
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Has a known history of corneal hypoesthesia (reduced corneal sensitivity)
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Has aphakia, keratoconus or a highly irregular cornea.
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Has Presbyopia or has dependence on spectacles for near work over the contact lenses.
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Has undergone corneal refractive surgery.
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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 fanfilcon A toric Fanfilcon A toric lens Subjects who wore fanfilcon A toric contact lens, either as the first or second lens in this cross-over study. lotrafilcon B Lotrafilcon B toric lens Subjects who wore lotrafilcon B toric contact lens, either as the first or second lens in this cross-over study.
- Primary Outcome Measures
Name Time Method Lens Centration 1 Month Centration of lens on eye in primary gaze (1-3 scale; 1=optimal centration, 2=Decentration acceptable, slightly, 3 = decentration unacceptable)
Corneal Coverage 1 Month Evaluate corneal coverage of contact lens (Yes=Full, No=Incomplete)
Post-blink Movement 1 Month Amount of lens movement after blink (0-4 scale, 0=insufficient, unacceptable movement, 2=optimal movement, 3=moderate, but acceptable movement 4=excessive, unacceptable movement)
Overall Fit Acceptance 1 Month Assessed by investigator based on lens fit alone (0-4 scale; 0=should not be worn, 4=perfect)
- Secondary Outcome Measures
Name Time Method Average Comfortable Wearing Time 1 Month Typical time of day when subject first experiences lens awareness or irritation
Average Hours of Wear Per Day 1 month Number of hours lenses are worn per day
Trial Locations
- Locations (1)
Optometry Clinic, National Autonomous University
🇲🇽Mexico City, Mexico