NCT06098937

Kalifilcon A Toric Compared to Commercially Available Lenses

Orientation Characteristics of Kalifilcon A Daily Disposable Toric Contact Lenses Compared to Commercially Available Daily Disposable Toric Contact Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 30 (actual)
• Sponsor: Bausch & Lomb Incorporated · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

Approximately thirty contact lens adapted subjects will be enrolled in this feasibility, bilateral, randomized, double masked (subject and investigator masked), repeated measures insertion study.

Detailed description

Approximately 30 soft toric contact lens adapted subjects will be enrolled in this feasibility, bilateral, randomized, double masked (subject and investigator masked), repeated measures insertion study. All subjects will be seen for a Screening/Dispensing Visit at which informed consent will be obtained and eligibility will be assessed. If study eligibility is met, subjects will have lenses inserted in random, successive order. Subjects will be receiving each of the study lens types once, in a randomized order. The subject will wear each of the study contact lenses for approximately 10 minutes.

Conditions

• Astigmatism

Interventions

Type	Name	Description
DEVICE	Kalifilcon Toric Lens	Kalifilcon A Daily Disposable Toric for Ametropia
DEVICE	Total1 for Astigmatism	Total1 for Astigmatism
DEVICE	Precision1 for Astigmatism	Precision1 for Astigmatism
DEVICE	MyDay Toric	MyDay Toric

Timeline

• Start date: 2023-09-05
• Primary completion: 2023-09-27
• Completion: 2023-09-27
• First posted: 2023-10-25
• Last updated: 2024-12-10
• Results posted: 2024-12-10

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study