NCT05959200

Clinical Performance Evaluation of Two Frequent Replacement Silicone Hydrogel Toric Contact Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 92 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The primary objective of this study is to evaluate the axis orientation of LID226397 toric contact lenses.

Detailed description

Subjects will be expected to attend 7 visits including a screening visit. The total duration of a subject's participation in the study will be approximately 40 days.

Conditions

• Ametropia
• Myopia
• Hyperopia
• Astigmatism

Interventions

Type	Name	Description
DEVICE	Serafilcon A toric contact lenses	Silicone hydrogel contact lenses for the optical correction of refractive ametropia (myopia or hyperopia with astigmatism)
DEVICE	Senofilcon A toric contact lenses	Silicone hydrogel contact lenses for the optical correction of refractive ametropia (myopia or hyperopia with astigmatism)
DEVICE	CLEAR CARE	Hydrogen peroxide-based contact lens cleaning and disinfecting solution

Timeline

• Start date: 2023-08-14
• Primary completion: 2023-10-23
• Completion: 2023-10-23
• First posted: 2023-07-25
• Last updated: 2024-11-29
• Results posted: 2024-11-29

Locations

7 sites across 1 country: United States