In-office Evaluation of Two Toric Soft Contact Lenses and a Spherical Soft Contact Lens

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

96 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-09-30

Study Completion Date

2007-11-30

Brief Summary

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The purpose of this study is to determine the relative performance of a new toric soft contact lens against a toric and a spherical contact lens currently available in market, specifically with regards to the fit and visual acuity as well as the comfort, vision and satisfaction while in the practitioner's office. Approximately 2 hours duration.

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Detailed Description

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Non-dispensing, single-masked (subject-masked), randomised, controlled study.

Conditions

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Astigmatism

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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senofilcon A/alphafilcon A/etafilcon A

First intervention:senofilcon A toric contact lenses Second intervention: alphafilcon A toric contact lenses Third intervention: etafilcon A sphere contact lenses

Group Type ACTIVE_COMPARATOR

senofilcon A toric contact lens

Intervention Type DEVICE

contact lens

alphafilcon A toric

Intervention Type DEVICE

contact lens

etafilcon A sphere

Intervention Type DEVICE

contact lens

alphafilcon A/etafilcon A/senofilcon A

First intervention: alphafilcon A toric contact lenses Second intervention: etafilcon A sphere contact lenses Third intervention: senofilcon A toric contact lenses

Group Type ACTIVE_COMPARATOR

senofilcon A toric contact lens

Intervention Type DEVICE

contact lens

alphafilcon A toric

Intervention Type DEVICE

contact lens

etafilcon A sphere

Intervention Type DEVICE

contact lens

etafilcon A/senofilcon A/alphafilcon A

First intervention: etafilcon A sphere contact lenses Second intervention:senofilcon A toric contact lenses Third intervention: alphafilcon A toric contact lenses

Group Type ACTIVE_COMPARATOR

senofilcon A toric contact lens

Intervention Type DEVICE

contact lens

alphafilcon A toric

Intervention Type DEVICE

contact lens

etafilcon A sphere

Intervention Type DEVICE

contact lens

senofilcon A/etafilcon A/alphafilcon A

First intervention: senofilcon A toric contact lenses Second intervention: etafilcon A sphere contact lenses Third intervention: alphafilcon A toric contact lenses

Group Type ACTIVE_COMPARATOR

senofilcon A toric contact lens

Intervention Type DEVICE

contact lens

alphafilcon A toric

Intervention Type DEVICE

contact lens

etafilcon A sphere

Intervention Type DEVICE

contact lens

alphafilcon A/senofilcon A/etafilcon A

First intervention: alphafilcon A toric contact lenses Second intervention: senofilcon A toric contact lenses Third intervention: etafilcon A sphere contact lenses

Group Type ACTIVE_COMPARATOR

senofilcon A toric contact lens

Intervention Type DEVICE

contact lens

alphafilcon A toric

Intervention Type DEVICE

contact lens

etafilcon A sphere

Intervention Type DEVICE

contact lens

etafilcon A/alphafilcon A/senofilcon A

First intervention: etafilcon A sphere contact lenses Second intervention: alphafilcon A toric contact lenses Third intervention: senofilcon A toric contact lenses

Group Type ACTIVE_COMPARATOR

senofilcon A toric contact lens

Intervention Type DEVICE

contact lens

alphafilcon A toric

Intervention Type DEVICE

contact lens

etafilcon A sphere

Intervention Type DEVICE

contact lens

Interventions

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senofilcon A toric contact lens

contact lens

Intervention Type DEVICE

alphafilcon A toric

contact lens

Intervention Type DEVICE

etafilcon A sphere

contact lens

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. be at least 18 and less than or equal to 39 years of age and have a need for vision correction in BOTH eyes (monovision or uniocular fitting is NOT allowed).
2. be of Asian descent (Japanese, Chinese, Korean, Polynesian or other Asian ancestry) and have Asian Eye anatomy
3. have successfully worn toric or spherical soft (hydrogel or silicone hydrogel) contact lenses for at least 4-weeks prior to enrollment in the study.
4. be able and willing to adhere to the instructions set forth in the protocol.
5. agree to wear their contact lenses in both eyes on a daily wear schedule for at least 8 hours per day every day during the study.
6. have a distance spherical component between -1.00 D and -5.50 D with cylinder in the range of 0.75 D to 2.25 D and cylinder axis within 10 ° of the vertical and within 20 ° of the horizontal in both eyes
7. have a best corrected manifest refraction visual acuity of at least 20/25 or better in each eye.
8. be in good general health, based on his/her knowledge.
9. read, be given an explanation of, indicate understanding of, and sign the STATEMENT OF INFORMED CONSENT.

Exclusion Criteria

1. The subject is a rigid gas permeable (RGP) or daily disposable soft lens wearer.
2. The presence of clinically significant (grade 3 or 4) anterior segment abnormalities; inflammations such as iritis; or any infection of the eye, lids, or associated structures.
3. The presence of ocular or systemic disease or need for medication which might interfere with contact lens wear or which would cause the lenses to be removed more than twice a day. (i.e., Sjögren's syndrome, type II diabetes, etc).
4. Slit lamp findings that would contraindicate contact lens wear such as:

* Pathological dry eye or associated findings
* Pterygium or corneal scars within the visual axis
* Neovascularization \>1mm in from the limbus
* History of giant papillary conjunctivitis (GPC) worse than Grade 2
* Anterior uveitis or iritis (past or present)
* Seborrhoeic eczema, seborrhoeic conjunctivitis
5. A history of recurrent erosions, corneal infiltrates, corneal ulcer or fungal infections.
6. A known history of corneal hypoesthesia (reduced corneal sensitivity.)
7. Aphakia, keratoconus or a highly irregular cornea.
8. Current pregnancy or lactation (to the best of the subject's knowledge).
9. Active participation in another clinical study at any time during this study.

Minimum Eligible Age

18 Years

Maximum Eligible Age

39 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No