Clinical Study of Visibility Tinted Clariti Contact Lens

Sauflon Pharmaceuticals

Status

Completed

Conditions

Myopia

Hyperopia

Treatments

Device: Clariti with Handling Tint

Device: Air Optix Aqua

Study type

Interventional

Funder types

Industry

Identifiers

NCT01996787

S13-540

Details and patient eligibility

About

The purpose of this study was to investigate the safety and efficacy of the Sauflon Clariti Monthly silicone hydrogel contact lenses with handling tint (Sauflon Pharmaceuticals Limited) by comparison with Air Optix Aqua silicone hydrogel lenses (Alcon Inc.)

Subjects used OptiFree Replenish solution (Alcon Lboratories Inc.) for daily lens maintenance, care and storage.

Full description

I. Study characteristics:

The clinical study evaluates the clinical performance of a silicone hydrogel contact lens for daily wear, Clariti (including handling tint) (Sauflon Pharmaceuticals Ltd.) versus a predicate device, Air Optix Aqua (Alcon Inc.), in terms of lens performance, physiological response and subjective acceptance.

Subjects used OptiFRee Replenish solution (Alcon Laboratories Inc.) for daily lens maintenance, care and storage.

The key features were as follows:

One month duration.
Three investigator sites.
Daily wear soft (hydrophilic) silicone hydrogel contact lenses, replaced on a monthly basis: Clariti Monthly (with handling tint)and Air Optix Aqua. Replenish was used as a care system by all subjects.
A total of 38 subjects were enrolled, and 38 subjects accounted for 76 eyes were dispensed lenses. This group was randomized into 25 test subjects (50 eyes) and 13 control subjects (26 eyes).
Of the 25 test subjects, 25 (100%) completed one month of use. Of the 13 control subjects, 12 (92.3%)completed one month of use.
There were no adverse reactions.

II. Study period:

The study was conducted over one month of wear. Subjects were examined initially, and at two follow-up visits after two weeks and four weeks respectively. Study visits commenced on June 26, 2013 and completed on September 14, 2013.

Enrollment

38 patients

Sex

All

Ages

19 to 56 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

They are 18 years of age and above
They understand their rights as a research subject and are willing and able to sign a Statement of Informed Consent
They are willing and able to follow the protocol
The agree not to paticipate in other clinical research for the duration of this study
They have a best spectacle corrected visual acuity greater or equal to 20/25 (logMAR 0.1)
They have a manifest cylinder less than or equal to 0.75D
They have successfully worn contact lenses within six months of starting the study
They can be fitted with spherical soft contact lenses within the power range available
They are willing to wear the study lenses for a minimum of four days a week, six hours a day

Exclusion criteria

They have any active anterior segment ocular disease which would normally contraindicate contact lens wear
They have any anterior segment infection, inflammation or abnormality
They use any systemic medications which would normally contraindicate contact lens wear
They are using any ocular medications
They have a history of herpetic keratitis
They have a systemic disorder which would normally contraindicate contact lens wear
They have any infectious disease (e.g. Hepatitis) or any immunosuppressive disease (e.g. HIV)
They have glaucoma (high pressure in the eye), have had cataract surgery or a history of recurring abrasions
They have had corneal refractive surgery or they have an irregular cornea
They have any corneal distortion resulting from previous hard or rigid lens wear or have keratoconus
They are pregnant or lactating
They have any slit lamp findings which are more serious than grade 1
They have a history of anaphylaxis or severe allergic reactions
They have taken part in any other contact lens or contact lens care product clinical trial or research, within two weeks prior to starting this study