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Performance of Toric Silicone Hydrogel Contact Lenses Following One Month of Daily Wear

Not Applicable
Completed
Conditions
Astigmatism
Interventions
Device: Fanfilcon A toric lens
Device: 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
Inclusion Criteria
  • 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
Exclusion Criteria

A person will be excluded from the study if he/she:

  • Has a CL prescription outside the range of the available parameters of the study lenses.

  • Has a spectacle cylinder less than -0.75D or more than -2.50 D of cylinder in either eye.

  • Has a history of not achieving comfortable CL wear (5 days per week; > 8 hours/day)

  • Has contact lens best corrected distance vision worse than 20/25 (0.10 logMAR) in either eye.

  • Presence of clinically significant (grade 2-4) anterior segment abnormalities

  • Presence of ocular or systemic disease or need of medications which might interfere with contact lens wear.

  • 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
  • Has a known history of corneal hypoesthesia (reduced corneal sensitivity)

  • Has aphakia, keratoconus or a highly irregular cornea.

  • Has Presbyopia or has dependence on spectacles for near work over the contact lenses.

  • Has undergone corneal refractive surgery.

  • Is participating in any other type of eye related clinical or research study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
fanfilcon A toricFanfilcon A toric lensSubjects who wore fanfilcon A toric contact lens, either as the first or second lens in this cross-over study.
lotrafilcon BLotrafilcon B toric lensSubjects who wore lotrafilcon B toric contact lens, either as the first or second lens in this cross-over study.
Primary Outcome Measures
NameTimeMethod
Lens Centration1 Month

Centration of lens on eye in primary gaze (1-3 scale; 1=optimal centration, 2=Decentration acceptable, slightly, 3 = decentration unacceptable)

Corneal Coverage1 Month

Evaluate corneal coverage of contact lens (Yes=Full, No=Incomplete)

Post-blink Movement1 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 Acceptance1 Month

Assessed by investigator based on lens fit alone (0-4 scale; 0=should not be worn, 4=perfect)

Secondary Outcome Measures
NameTimeMethod
Average Comfortable Wearing Time1 Month

Typical time of day when subject first experiences lens awareness or irritation

Average Hours of Wear Per Day1 month

Number of hours lenses are worn per day

Trial Locations

Locations (1)

Optometry Clinic, National Autonomous University

🇲🇽

Mexico City, Mexico

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