Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens

Completed · Not applicable

Conditions studied: Corneal Deformity

In brief

This will be a randomized non-dispensing study comparing the overnight corneal swelling of an eye while wearing no contact lens to the Ultra contract lens.

Key facts

Study ID

NCT02258139

Run by

Bausch & Lomb Incorporated

People needed

38

Starts

2014-11-03

Expected to finish

2014-12-11

Last updated by the study team

2020-09-14

Who can join

Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Be between 18 and 40 years of age (inclusive)
• Not a current contact lens wearer (have not worn extended wear, and not worn in lenses in 6 months)
• Able to read, comprehend and sign an informed consent
• Willing to comply with the wear and study visit schedule
• Monocular best-corrected distance visual acuity >/-20/25 in each eye

You may not qualify if…

• Any active corneal infection, disease, injury, inflammation, past surgery, or ocular abnormality which may interfere with contact lens wear
• Systemic or ocular allergies, which might interfere with contact lens wear
• Systemic disease or condition, which might interfere with contact lens wear
• Use of prescription sleep aids or alcohol within 24 hours of study appointment
• Inability to wear contact lenses
• Under 18 years of age

Where it is running

• Indiana University — Bloomington, Indiana, United States

Full record on ClinicalTrials.gov

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