A Range of Contact Lenses and Care System Combinations

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

28 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-09-12

Study Completion Date

2018-12-12

Brief Summary

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The objective of this study is to compare the short-term clinical response to all combinations of two lens types: fanfilcon A and comfilcon A with two care systems: Hy-Care and Lite. The primary variables of interest are short-term biomicroscopy signs. Other variables of interest include subjective response and visual performance.

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Detailed Description

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Subjects were randomized to wear fanfilcon A soft contact lens in one eye and comfilcon A soft contact lens in the other eye with each lens having been soaked overnight in the Hy-Care contact lens solution and Lite contact lens solution.

Conditions

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Contact Lens Solutions

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

This is a double-masked, randomized, contralateral, crossover study design. Lenses are worn as an unmatched pair.

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Investigators

The first solution, the randomisation determines that the right lens will wear the fanfilcon A lens and the left eye will wear the comfilcon A lens for two hours of wear, with a two-day 'wash-out' period and the laterality of the lenses will be swapped for the second solution for two hours of wear. Lenses will be provided in lens cases which do not detail lens or care system information.

Study Groups

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Hy-Care Contact Lens Solution

Each subject will wear fanfilcon A soft contact lens in one eye and comfilcon A soft contact lens in the other eye with each lens having been soaked overnight in the Hy-Care contact lens solution.

Group Type ACTIVE_COMPARATOR

Hy-Care Contact Lens Solution

Intervention Type DEVICE

Hy-Care Contact Lens Solution

fanfilcon A soft contact lens

Intervention Type DEVICE

fanfilcon A soft contact lens

comfilcon A soft contact lens

Intervention Type DEVICE

comfilcon A soft contact lens

Lite Contact Lens Solution

Each subject will wear fanfilcon A soft contact lens in one eye and comfilcon A soft contact lens in the other eye with each lens having been soaked overnight in the Lite contact lens solution.

Group Type ACTIVE_COMPARATOR

Lite Contact Lens Solution

Intervention Type DEVICE

Lite Contact Lens Solution

fanfilcon A soft contact lens

Intervention Type DEVICE

fanfilcon A soft contact lens

comfilcon A soft contact lens

Intervention Type DEVICE

comfilcon A soft contact lens

Interventions

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Hy-Care Contact Lens Solution

Intervention Type DEVICE

Lite Contact Lens Solution

Intervention Type DEVICE

fanfilcon A soft contact lens

Intervention Type DEVICE

comfilcon A soft contact lens

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. They are of legal age (18) and capacity to volunteer.
2. They understand their rights as a research subject and are willing and able to sign a Statement of Informed Consent.
3. They are willing and able to follow the protocol.
4. They agree not to participate in other clinical research for the duration of this study.
5. They can be satisfactorily fitted with the study lens for a period of approximately 2 hours.
6. They can attain at least 0.20 logMAR distance high contrast visual acuity in each eye with their habitual spectacles.
7. They currently wear daily disposable soft contact lenses or have done so in the previous six months.
8. They are willing to comply with the wear schedule (approximately 2 hours on two different days)
9. They own a wearable pair of spectacles and agree to bring these to study visits.

Exclusion Criteria

1. They have an ocular disorder which would normally contra-indicate contact lens wear.
2. They have a systemic disorder which would normally contra-indicate contact lens wear.
3. They currently wear reusable soft contact lenses in both eyes.
4. They are using any topical medication such as eye drops or ointment.
5. They have had cataract surgery.
6. They have had corneal refractive surgery.
7. They have any corneal distortion resulting from previous hard or rigid lens wear or have keratoconus.
8. They are pregnant or breast-feeding.
9. They have any ocular abnormality which would, in the opinion of the investigator, normally contraindicate contact lens wear.
10. They have Type 2 or greater corneal staining prior to lens application at Visit 1 or 2
11. They have corneal staining covering greater than 20% in any corneal region at Visit 1a or 2a
12. They have any infectious disease which would, in the opinion of the investigator, contraindicate contact lens wear or pose a risk to study personnel; or they have any immunosuppressive disease (e.g. HIV), or a history of anaphylaxis or severe allergic reaction.
13. They have taken part in any other contact lens or care solution clinical trial or research, within two weeks prior to starting this study.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No