A Comparative Study of Two Daily Disposable Contact Lenses in Higher Myopia Subjects

Alcon

Status: Completed

Conditions: Myopia; Refractive Error

Treatments: Device: Narafilcon A contact lens; Device: Delefilcon A contact lens; Device: Spectacles

Study type: Interventional

Funder types: Industry

Identifiers

NCT02066922

C-12-057

Details and patient eligibility

About

The purpose of this study is to compare the change from baseline in central corneal curvature at one week, between 2 silicone hydrogel lenses, in higher myopic subjects.

Full description

Participants were expected to attend 4 office visits. Visit 1 was the Screening/Enrollment visit. At Visit 2 (Baseline Visit), participants were randomized and the study lenses were trial fit. At Visit 3 (Dispense Visit), participants received study lenses for approximately 1 week of wear. Visit 4 was the Exit visit. Expected duration of participation in the study was 3 weeks.

Enrollment: 19 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Sign Informed Consent document;
• Higher degree of myopia in both eyes, i.e. habitual contact lens power between -10.00 diopters (D) and -17.00D;
• Best corrected distance visual acuity greater than or equal to 20/30 in each eye (measured with either spectacle refraction or habitual contact lenses plus over refraction);
• Manifest astigmatism less than or equal to -1.00D;
• Soft contact lens wear in both eyes at least 5 days per week and at least 8 hours per day;
• Other protocol-defined inclusion criteria may apply.

Exclusion criteria

• Pregnant or lactating;
• Eye injury or surgery within twelve weeks immediately prior to enrollment;
• Any ocular condition that contraindicates contact lens wear;
• History of herpetic keratitis;
• Any use of systemic or ocular medications for which contact lens wear could be contraindicated, including any use of topical ocular medications that would require instillation during contact lens wear, except for approved lubricating drops;
• Clinical significant dry eye not responding to treatment;
• Previous corneal or refractive surgery or irregular cornea;
• Requires reading glasses;
• Participation in a clinical trial (including contact lens or contact lens care product) within the previous 30 days;
• Wears habitual lenses in an extended wear modality (routinely sleeps in lenses overnight for 1 night per week or more) over the last 3 months prior to enrollment;
• Other protocol-defined exclusion criteria may apply.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: Double Blind

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19 participants in 2 patient groups

DAILIES TOTAL1

Experimental group

Description:

Delefilcon A contact lens randomly assigned to one eye, with narafilcon A contact lens in the fellow eye for contralateral wear. Both products worn in a daily wear, daily disposable mode approximately 8 hours a day for approximately 1 week, with spectacles worn over contact lenses if needed to provide acceptable vision.

Treatment:

Device: Delefilcon A contact lens

Device: Spectacles

Device: Narafilcon A contact lens

TRUEYE

Active Comparator group

Description:

Narafilcon A contact lens randomly assigned to one eye, with delefilcon A contact lens in the fellow eye for contralateral wear. Both products worn in a daily wear, daily disposable mode approximately 8 hours a day for approximately 1 week, with spectacles worn over contact lenses if needed to provide acceptable vision.

Treatment:

Device: Delefilcon A contact lens

Device: Spectacles

Device: Narafilcon A contact lens