Clinical Trials Directory

Trials / Completed

CompletedNCT02258139

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

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
38 (actual)
Sponsor
Bausch & Lomb Incorporated · Industry
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DEVICEB&L Investigational Contact LensThe lens used in this study will be supplied by the Sponsor. All subjects will wear a -3.00D lens.

Timeline

Start date
2014-11-03
Primary completion
2014-12-11
Completion
2014-12-11
First posted
2014-10-07
Last updated
2020-09-14
Results posted
2020-09-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02258139. Inclusion in this directory is not an endorsement.

Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens (NCT02258139) · Clinical Trials Directory