NCT05313412

Clinical Evaluation of Two Silicone Hydrogel Contact Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 38 (actual)
• Sponsor: CooperVision, Inc. · Industry
• Sex: All
• Age: 18 Years – 40 Years
• Healthy volunteers: Accepted

Summary

This study is to compare the short-term clinical performance and subjective acceptance of two silicone hydrogel soft contact lenses.

Detailed description

This is a double-masked, randomized, bilateral crossover study to compare the short-term clinical performance of two silicone hydrogel soft contact lenses. Each lens type is worn for approximately six hours on separate study days, in random sequence.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	Lens A (comfilcon A lens)	6 hours
DEVICE	Lens B (lehfilcon A lens)	6 hours

Timeline

• Start date: 2022-01-27
• Primary completion: 2022-04-21
• Completion: 2022-04-21
• First posted: 2022-04-06
• Last updated: 2023-05-09
• Results posted: 2023-05-09

Locations

1 site across 1 country: United Kingdom

Regulatory

• FDA-regulated device study