Clinical Performance of the OxyAqua Daily Disposable Silicone Hydrogel Soft Contact Lens

Visco Vision

Status

Completed

Conditions

Myopia

Treatments

Device: Si-Hy

Device: OxyAqua

Study type

Interventional

Funder types

Industry

Identifiers

NCT03139201

1040625M

Details and patient eligibility

About

The objective of this study is to demonstrate that the OxyAqua silicone hydrogel soft contact lens could be prescribed as a supportive care for myopes.

Full description

This is a double blind randomized control study to evaluate a daily disposable contact lens. It is planned to have 30 evaluable subjects at least divided evenly among 3 independent PIs from one hospital. Each PI will enroll 12 subjects at least. The ration of evaluable test subjects to control subjects will be 2 to 1. The study lens will be dispensed randomly to subjects who have normal ocular health and conform to a set of criteria. It is necessary to wear the lens 8 hours a day and 5 days a week at least and follow up for one month (30 days). Data will be collected at baseline, 1 week, 2 week and 4 week of daily disposable modality including Adverse Reactions, Slit-lamp findings and Symptoms, Problems, and Complaints, vision acuity, keratometry change and reason for discontinuation.

Enrollment

36 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects should have normal eyes and use no ocular medications. They may have worn contact lenses previously, provided their eyes are shown to be normal at the start of the investigation. A normal eye is defined as having the following characteristics:
1. No anterior segment infection, inflammation or abnormality.
2. No other active ocular or systemic disease that would contraindicate contact lens wear; and
3. No medications that would contraindicate contact lens wear.
VA correctable to 0.1 LogMAR or better, with spherical lenses ranging in power from
1.00 to -10.00 D myopia, astigmatism less than 2.00 D
Willing to comply with all study procedures and be available for the duration of the study.
Provide signed and dated informed consent form.

Exclusion criteria

Have history of allergies that would contraindicate "normal" contact lens wear.
Have other active ocular or systemic disease such as, but not limited to: anterior uveitis (past or present), glaucoma, Sjögren's syndrome, lupus erythematosus, sclerodermas, keratoconus or type II diabetes, slip lamp findings greater than grade I (such as cornea or interstitial edema).
Have medications that would contraindicate contact lens wear.
Have had any cornea surgery.
Currently pregnant (to the best of the subject's knowledge), is lactating or is planning a pregnancy within the next 1 month.
Any active participation in another clinical trial within 30 days prior to this study.
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.
A known history of corneal hypoesthesia (reduced corneal sensitivity), corneal ulcer, corneal infiltrates or fungal infections.
A history of papillary conjunctivitis that has interfered with contact lens wear.
No monocular or monovision fits.
Alcoholic or Drug Abused.