Dry Eye Clinical Trial
Official title:
Direct Application of Systane Complete to Contact Lenses for the Treatment of Contact Lens Discomfort
Verified date | October 2020 |
Source | University of Alabama at Birmingham |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A common first line treatment for patients with dryness symptoms or contact lens discomfort is the application of artificial tears or rewetting drops, respectively. Rewetting drops are specifically formulated for use with contact lenses while artificial tears are indicated for dry eye. Modern rewetting drops and artificial tears have similar formulations with similar preservatives, preservatives that have been shown to be compatible with contact lenses. While rewetting drops and artificial tears are regulated under different U.S. Food & Drug Administration policies, artificial tears are not specifically indicated for direct use with contact lenses. Nevertheless, clinicians commonly prescribe artificial tears to contact lens wearers likely because newer formulations of artificial tear have the potential to outperform available rewetting drops. The safety and efficacy of using artificial tears with contact lenses for the treatment of discomfort is supported by Caffery and Josephson and Ozkan and Papas who found that artificial tears significantly reduces dryness symptoms in contact lens wearers. Thus, the purpose of this study is to test the safety of directly applying a new artificial tear, Systane Complete, to the contact lens wearing eye and its ability to alleviate symptoms while wearing contact lenses during the day.
Status | Completed |
Enrollment | 73 |
Est. completion date | October 20, 2019 |
Est. primary completion date | October 20, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Daily disposable contact lens wearers - 20/30 visual acuity or better - Self-report contact lens discomfort - Contact Lens Dry Eye Questionnaire (CLDEQ)-8 scores = 12 Exclusion Criteria: - Other contact lens modalities/wear schedules (e.g., two week and monthly replacement CLs, gas permeable CLs) - Non-compliant daily disposable contact lens wearers - Systemic health conditions that alter tear film physiology (e.g., primary and secondary Sjögren's syndrome) - History of ocular surgery within the past 12 months - History of severe ocular trauma - History of active ocular infection or inflammation - Isotretinoin-derivatives use - Ocular medication use - Pregnant or breast feeding |
Country | Name | City | State |
---|---|---|---|
United States | Lindenhurst Eye Physicians & Surgeons, P.C. | Babylon | New York |
United States | University of Alabama at Birmingham | Birmingham | Alabama |
United States | Southern College of Optometry | Memphis | Tennessee |
Lead Sponsor | Collaborator |
---|---|
University of Alabama at Birmingham | Alcon Research |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Difference in Ocular Surface Damage as Measured by the Brien Holden Vision Institute (BHVI Grading Scale) at Two Weeks | The Corneal Staining Scores are measured by the BHVI grading scale. The grading scales are a quick reference to the key signs associated with contact lens related inflammation and infection. Used as a reference tool in the clinic, they provide a guide for determining how much normal ocular appearance has changed in a patient, and can help inform clinical management decisions. The range of the scores are: 0-4 in five regions (total sum score = 20). A lower score indicates a better outcome. | 2 Weeks | |
Secondary | Identifying Contact Lens (CL) Participants With Dry Eye Disease (DED), as Measured by the Contact Lens Dry Eye Questionnaire-4 Items (CLDEQ-4) Between Two Weeks and Baseline. | The CLDEQ-4 is a contact lens specific symptoms survey; range = 0-18 with 18 being most symptomatic. | 2 Weeks |
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