Status:
COMPLETED
Comparison of Two Toric Contact Lenses on Current Toric Wearers
Lead Sponsor:
Johnson & Johnson Vision Care, Inc.
Conditions:
Ametropia
Eligibility:
All Genders
18-45 years
Phase:
NA
Brief Summary
The purpose of this study is to evaluate and compare the clinical performance of two toric contact lenses amongst 110 subjects, 2-week, single masked (subject), daily wear, randomized, bilateral, cros...
Detailed Description
Up to 7 sites in the US will participate. Each investigator will have both test and control lens types. There will be a maximum of 6 scheduled visits: Visit 1: Habitual lens evaluation / Baseline / T...
Eligibility Criteria
Inclusion
- Be at least 18 and less than or equal to 45 years of age, have a need for vision correction and wear contact lenses in BOTH eyes (monovision or uni-ocular fitting is NOT allowed).
- Be able to read J1 at near WITHOUT the aid of a near addition over the distance prescription.
- Be a currently successful wearer for at least 3 months of B\&L SofLens 66 Toric hydrogel lenses.
- Be able and willing to adhere to the instructions set forth in the protocol.
- 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.
- Have a distance spectacle spherical component between -1.00 D and -5.25 D with cylinder in the range of 0.75 D to 2.25 D and cylinder axis within 10 ° of the vertical and within 30° of the horizontal in both eyes (when the subject's prescription is presented in minus cylinder form).
- Have a best corrected manifest refraction visual acuity of at least 20/25 or better in each eye.
- Be in good general health, based on his/her knowledge.
- Must be given an explanation of the study objectives, lens and solutions usage requirements and visit schedule. The subject must read, indicate understanding of and agree to begin participation in the clinical study. The subject must then sign the Informed Consent Form in the presence of the Investigator or their designee.
Exclusion
- Presbyopic or has the need for a near add for reading.
- Previous refractive surgery; current or previous orthokeratology treatment.
- Aphakia, keratoconus or a highly irregular cornea.
- The presence of ocular or systemic disease or has the need for medication (ocular or systemic) which might interfere with contact lens wear or which would cause the lenses to be removed more than twice a day. (e.g., Sjögren's syndrome, type II diabetes, allergies).
- A known history of corneal hypoesthesia (reduced corneal sensitivity.)
- Anterior uveitis or iritis (past or present).
- A history of recurrent erosions, corneal infiltrates corneal ulcer or fungal infections.
- Clinically significant (grade 3 or 4) anterior segment abnormalities; inflammations or infections of the eye, eyelids, or associated structures.
- 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
- Meibomian gland dysfunction, blepharitis, or seborrhoeic dermatitis
- Current pregnancy or lactation (to the best of the subject's knowledge).
- Actively participating in another clinical study at any time during this study.
Key Trial Info
Start Date :
February 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2008
Estimated Enrollment :
89 Patients enrolled
Trial Details
Trial ID
NCT00639379
Start Date
February 1 2008
End Date
June 1 2008
Last Update
May 21 2015
Active Locations (7)
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1
Ted Brink and Associates
Jacksonville, Florida, United States, 32256
2
Eola Eyes
Orlando, Florida, United States, 32801
3
Clayton Eye Center
Morrow, Georgia, United States, 30260
4
The Koetting Associates Inc.
St Louis, Missouri, United States, 63144