NCT03560141

Clinical Performance of a Silicone Hydrogel Contact Lens Following One Night of Extended Wear

Clinical Performance of a Silicone Hydrogel Following One Night of Extended Wear

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 12 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this clinical study is to evaluate the on-eye performance of an investigational soft contact lens compared to a commercially available soft contact lens following 1 night of extended wear.

Detailed description

Subjects will be randomized to wear the investigational contact lens in 1 eye and the commercially available contact lens in the other eye. Subjects will be expected to attend 4 scheduled study visits. The lenses will be worn continuously from the time of dispense on Day 1 until lens collection at the Day 2 Follow-up/Exit Visit.

Conditions

• Refractive Errors

Interventions

Type	Name	Description
DEVICE	LID011121 contact lens	Investigational silicone hydrogel contact lens
DEVICE	Comfilcon A contact lens	Commercially available silicone hydrogel contact lens

Timeline

• Start date: 2018-07-11
• Primary completion: 2018-07-17
• Completion: 2018-07-17
• First posted: 2018-06-18
• Last updated: 2021-07-28
• Results posted: 2021-07-28

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study