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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06462456
Other study ID # CLE383-I001
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date August 2024
Est. completion date December 2027

Study information

Verified date June 2024
Source Alcon Research
Contact Alcon Call Center
Phone 1-888-451-3937
Email alcon.medinfo@alcon.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess long term performance and safety of verofilcon A soft contact lenses in a real-world setting in a population of 7 years or older having at least 1 year of verofilcon A (sphere or toric) contact lens wear in a daily wear and daily disposable modality.


Description:

This study consists of a Baseline Visit and a Year 1 Visit. The Baseline Visit is defined as the first office visit where an eye care professional provided an in-person office biomicroscopy exam to the subject before or during which a PRECISION1™ sphere or toric contact lens prescription was released. The Baseline Visit will be retrospective, with all assessments obtained from chart review. The Year 1 Visit is defined as the visit that occurs 1 year (-2/+4 months) since Baseline during which period the subject is wearing test lenses of the same design in both eyes and a contact lens examination is performed during the visit. The Year 1 Visit may be prospective or retrospective.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 168
Est. completion date December 2027
Est. primary completion date December 2027
Accepts healthy volunteers No
Gender All
Age group 7 Years and older
Eligibility Key Inclusion Criteria: - Subject (or subject's legal representative) is able to understand and sign an informed consent/assent form approved by an Institutional Review Board (IRB), unless appropriate consent waiver for the retrospective chart review is provided by the IRB. - Verofilcon A (sphere or toric) contact lens wear as described in the protocol. - Best corrected spectacle distance visual acuity (VA) 20/25 or better at baseline. - Healthy, non-diseased eyes, as determined/known by the Investigator. - Other protocol-defined inclusion criteria may apply. Key Exclusion Criteria: - Any ocular disease or condition that would contraindicate contact lens wear present at baseline. - Use of systemic or ocular medications that would contraindicate contact lens wear at baseline. - Other protocol-defined exclusion criteria may apply.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Verofilcon A spherical soft contact lenses
Silicone hydrogel contact lenses prescribed for single use, daily disposable wear (less than 24 hours while awake) for the correction of ametropia (myopia or hyperopia)
Verofilcon A toric soft contact lenses
Silicone hydrogel contact lenses prescribed for single use, daily disposable wear (less than 24 hours while awake) for the correction of ametropia (myopia or hyperopia) with astigmatism

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Alcon Research

Outcome

Type Measure Description Time frame Safety issue
Primary Distance Visual Acuity with Study Lenses at Baseline Visual acuity (VA) assessed per the investigator's standard of care with study lenses in place. Baseline
Primary Distance Visual Acuity with Study Lenses at Year 1 Follow-Up Visual acuity (VA) assessed per the investigator's standard of care with study lenses in place. Year 1
Primary Incidence of Corneal Infiltrative Events A corneal infiltrate is a single or group of inflammatory cells in the normally clear cornea. Up to Year 1
Primary Incidence of Microbial Keratitis Microbial keratitis is a sight-threatening infection of the cornea. Up to Year 1
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