Clinical Evaluation of Invigor Toric 1-Day Contact Lenses
- Conditions
- Astigmatism
- Interventions
- Device: 1-day toric test contact lensDevice: 1-day toric control contact lens
- Registration Number
- NCT04016623
- Lead Sponsor
- Coopervision, Inc.
- Brief Summary
An evaluation of the clinical performance of the 1-day toric test contact lens compared to the 1-day toric control contact lens over one hour of lens wear.
- Detailed Description
A non-dispensing, double-masked, randomized, contralateral study comparing the 1-day toric test contact lens against the 1-day toric control contact lens to evaluate the clinical performance over one hour of lens wear. Each subject will be randomized to wear the test lens in one eye and the control lens in the other eye for each pair of lenses.
Each subject will be asked to wear four pairs of contact lenses in the study
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 10
- Has had a self-reported oculo-visual examination in the last two years.
- Is at least 18 years of age and has full legal capacity to volunteer.
- Has read and understood the information consent letter.
- Is willing and able to follow instructions and maintain the appointment schedule.
- Is correctable to a visual acuity of 20/40 or better (in each eye) with their habitual vision correction or 20/20 best-corrected.
- Currently wears soft contact lenses.
- Has clear corneas and no active ocular disease.
- Has not worn lenses for at least 12 hours before the examination
- 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 affect the wearing of contact lenses.
- Has persistent, clinically significant corneal or conjunctival staining using sodium fluorescein dye.
- Has any clinically significant lid or conjunctival abnormalities, active neovascularization or any central corneal scars.
- Is aphakic.
- 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
- FACTORIAL
- Arm && Interventions
Group Intervention Description 1-day toric test contact lens 1-day toric test contact lens Each subject will wear the 1-day toric test (Test) lens in one eye and 1-day toric control (Control) contact lens in the other eye. Patient will wear as an unmatched pair, per predetermined randomization schedule (to determine which eye receives the Test or Control contact lens). 1-day toric test contact lens 1-day toric control contact lens Each subject will wear the 1-day toric test (Test) lens in one eye and 1-day toric control (Control) contact lens in the other eye. Patient will wear as an unmatched pair, per predetermined randomization schedule (to determine which eye receives the Test or Control contact lens). 1-day toric control contact lens 1-day toric test contact lens Each subject will wear the 1-day toric test (Test) lens in one eye and 1-day toric control (Control) contact lens in the other eye. Patient will wear as an unmatched pair, per predetermined randomization schedule (to determine which eye receives the Test or Control contact lens). 1-day toric control contact lens 1-day toric control contact lens Each subject will wear the 1-day toric test (Test) lens in one eye and 1-day toric control (Control) contact lens in the other eye. Patient will wear as an unmatched pair, per predetermined randomization schedule (to determine which eye receives the Test or Control contact lens).
- Primary Outcome Measures
Name Time Method Toric Fit Preference 1 hour Investigator's toric fitting preference - Test lens, No Preference, Control lens.
Data for all 4 pairs were combined and analyzed (n=40 contact lenses).Visibility of Toric Mark 1 hour Toric Mark visible or not visible. Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
Degree of Rotational Recovery 1 hour Rotational Recovery for nasal and temporal - measured in degrees. Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
Toric Fit Acceptance 1 hour Toric fit acceptance and preference scale 0-4 (0 = can't be worn, 4 = optimum). Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
Degree of Lens Orientation 1 hour Average of lens toric mark mislocation from the resting toric mark away from the 6 o'clock position - measured in degrees.
Data for all 4 pairs were combined and analyzed (n=40 contact lenses).Toric Stability 1 hour Rotational stability (maximal and minimal differences between extreme gazes) measured in degrees for up, down, right, and left gazes.
Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
- Secondary Outcome Measures
Name Time Method Lens Push-Up 1 hour Lens push-up measured in percentage. Data for all 4 pairs were combined and analyzed (n=40 control lenses).
Primary Lens Gaze Lag 1 hour Primary lens gaze lag measured in millimeters. Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
Measurement of Lens Movement 1 hour Measurement of lens movement in millimeters. Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
Measurement of Lens Horizontal Centration 1 hour Measurement of Lens Horizontal Centration in millimeters. Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
General Lens Fit Acceptance 1 hour General lens fit acceptance and preference scale 0-4 (0 = unacceptable, 4 = optimal).
Data for all 4 pairs were combined and analyzed (n=40 contact lenses).Measurement of Lens Vertical Centration 1 hour Lens Horizontal centration measured in mm. Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
Up Gaze Lag 1 hour Up gaze lag measured in millimeters. Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
General Lens Fit Preference 1 hour Investigator's general lens fit preference - Test lens, No preference, Control lens.
Data for all 4 pairs were combined and analyzed (n=40 contact lenses).
Trial Locations
- Locations (1)
Clinical Optics Research Lab (CORL) Indiana University School of Optometry, Indiana University
🇺🇸Bloomington, Indiana, United States