Refractive Errors Clinical Trial
Official title:
Post-market Clinical Follow-up Study of Alcon PRECISION1™ Spherical Soft Contact Lenses (Verofilcon A) and PRECISION1T™ for Astigmatism Contact Lenses (Verofilcon A)
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.
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. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Alcon Research |
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 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04532099 -
Clinical Comparison of Two Daily Wear Frequent Replacement Silicone Hydrogel Soft Contact Lenses
|
N/A | |
Completed |
NCT05039112 -
Clinical Comparison of 2 Daily Disposable Toric Soft Contact Lenses
|
N/A | |
Completed |
NCT03670303 -
Trial of an Educational Intervention to Promote Spectacle Use Among Secondary School Children in Islamabad, Pakistan
|
N/A | |
Completed |
NCT02255474 -
Bifocal Lenses In Nearsighted Kids
|
N/A | |
Not yet recruiting |
NCT03222661 -
Direct Comparison of SVOne Obtained Refraction to Subjective Manifest Refraction
|
N/A | |
Completed |
NCT04055519 -
Clinical Performance Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens
|
N/A | |
Recruiting |
NCT05049070 -
Study to Evaluate the Reliability, Validity and Safety of Subjective Mobile Refraction
|
N/A | |
Completed |
NCT04527978 -
Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 1
|
N/A | |
Completed |
NCT01430247 -
Vision Screening for the Detection of Amblyopia
|
N/A | |
Recruiting |
NCT06077682 -
Cycloplegic Refraction in Pediatric Patients With Esotropia
|
Phase 4 | |
Not yet recruiting |
NCT04077086 -
Correcting Myopia Among Secondary School Children to Increase Academic High School Attendance Rates in Rural Communities
|
N/A | |
Withdrawn |
NCT04352868 -
Customizing Myopia Control With Multifocal Toric Contact Lens
|
N/A | |
Completed |
NCT04528017 -
Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 2
|
N/A | |
Recruiting |
NCT04338880 -
Academic Performance and Refractive Error
|
||
Recruiting |
NCT04545073 -
Outcomes of a Trifocal IOL in Post-refractive Patients
|
||
Enrolling by invitation |
NCT05992675 -
Air Optix® Night and Day® Aqua Continuous Wear
|
||
Enrolling by invitation |
NCT05976750 -
Air Optix® Night and Day® Aqua Daily Wear
|
||
Recruiting |
NCT04693247 -
Handheld Device Compared With a Standard Eye Care Diagnostic Device in Measuring Ophthalmic Refraction
|
N/A | |
Recruiting |
NCT06065631 -
Seeing to Learn in Sierra Leone
|
N/A | |
Not yet recruiting |
NCT05550740 -
Repeated Low-Level Red-Light Therapy for Shortening Axial Length
|
N/A |