- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05827224
Air Optix Daily Wear Contact Lenses
April 1, 2024 updated by: Alcon Research
The purpose of this Post-Market Clinical Follow-Up (PMCF) study is to assess long term performance and safety of Air Optix Aqua, Air Optix plus HydraGlyde Sphere, and Air Optix plus HydraGlyde Toric soft contact lenses in a real-world setting when worn as daily wear.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This is a non-interventional/observational study designed as a retrospective chart review.
Study sites will identify charts within their existing databases in a fair and consistent manner, e.g., reviewing all eligible charts in reverse chronological order by year of baseline visit.
The baseline visit will be defined as the first office visit where an eye care practitioner provided an in-person office biomicroscopy exam to the patient, before or during which a contact lens prescription for the study or comparator contact lenses was released.
Subjects meeting the eligibility criteria will be enrolled in the study.
Study Type
Observational
Enrollment (Actual)
276
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Alcon Call Center
- Phone Number: 1-888-451-3937
- Email: medinfo.alcon@alcon.com
Study Locations
-
-
Florida
-
Orlando, Florida, United States, 32803
- Vision Health Institute
-
-
Minnesota
-
Medina, Minnesota, United States, 55340
- Complete Eye Care of Medina
-
-
Missouri
-
Saint Louis, Missouri, United States, 63144
- Koetting Associates
-
-
Tennessee
-
Nashville, Tennessee, United States, 37215
- Toyos Clinic
-
-
Utah
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Salt Lake City, Utah, United States, 84117
- Smith Bowman Ophthalmology
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Investigators will enroll charts following a pre-identified process.
Description
Key Inclusion Criteria:
- Manifest refraction cylinder less than or equal to 0.75 diopter (D) in each eye at baseline (sphere wearers only);
- Best corrected visual acuity (BCVA) of 20/25 Snellen or better in each eye at baseline;
- Must have worn or be wearing Air Optix Aqua Sphere, Air Optix plus HydraGlyde Sphere, Air Optix plus HydraGlyde Toric, Biofinity Sphere or Biofinity Toric for at least 1 year in a daily wear modality, as determined by the Investigator;
- Other protocol-defined inclusion criteria may apply.
Key Exclusion Criteria:
- Have worn or be wearing Air Optix Aqua Sphere, Air Optix plus HydraGlyde Sphere, Air Optix plus HydraGlyde Toric, Biofinity Sphere, or Biofinity Toric contact lenses in an extended wear modality;
- Any recurrent history or active anterior segment infection, inflammation or abnormality contraindicating regular contact lens wear at baseline;
- Use of systemic or ocular medications contraindicating regular contact lens wear at baseline and/or during the period of the retrospective chart collection;
- Slit lamp findings, including signs of pathological dry eye, that would contraindicate regular contact lens wear;
- Other protocol-defined exclusion criteria may apply.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Air Optix Aqua Sphere
Lotrafilcon B spherical soft contact lenses worn in both eyes and removed daily for cleaning and disinfection
|
Commercially available silicone hydrogel contact lenses
Other Names:
|
Air Optix plus HydraGlyde Sphere
Lotrafilcon B spherical soft contact lenses with comfort additive worn in both eyes and removed daily for cleaning and disinfection
|
Commercially available silicone hydrogel contact lenses
Other Names:
|
Air Optix plus HydraGlyde Toric
Lotrafilcon B toric soft contact lenses with comfort additive worn in both eyes and removed daily for cleaning and disinfection
|
Commercially available silicone hydrogel contact lenses
Other Names:
|
Biofinity Sphere
Comfilcon A spherical soft contact lenses worn in both eyes and removed daily for cleaning and disinfection
|
Commercially available silicone hydrogel contact lenses
Other Names:
|
Biofinity Toric
Comfilcon A toric soft contact lenses worn in both eyes and removed daily for cleaning and disinfection
|
Commercially available silicone hydrogel contact lenses
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Distance visual acuity (VA) with study lenses
Time Frame: Up to Year 1
|
The subject's chart will be reviewed for distance visual acuity at baseline and at 1 year following the baseline exam.
|
Up to Year 1
|
Incidence of corneal infiltrative events
Time Frame: Up to Year 1
|
The subject's chart will be reviewed for incidences of corneal infiltrative events occurring after the baseline exam.
|
Up to Year 1
|
Incidence of microbial keratitis
Time Frame: Up to Year 1
|
The subject's chart will be reviewed for incidences of microbial keratitis occurring after the baseline exam.
|
Up to Year 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Clinical Trial Lead, Vision Care, Alcon Research, LLC
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 2, 2023
Primary Completion (Actual)
December 13, 2023
Study Completion (Actual)
December 13, 2023
Study Registration Dates
First Submitted
April 13, 2023
First Submitted That Met QC Criteria
April 13, 2023
First Posted (Actual)
April 24, 2023
Study Record Updates
Last Update Posted (Actual)
April 2, 2024
Last Update Submitted That Met QC Criteria
April 1, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CLJ241-N001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
Yes
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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