Clinical Trials Directory

Trials / Completed

CompletedNCT01100424

Assessment of Tear Film-Based Proteins Associated With Care Solution Induced Corneal Staining

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

The purpose of this study was to investigate the association of inflammatory mediators found in the tear film during the development and following the induction of contact lens solution-induced corneal staining.

Conditions

Interventions

TypeNameDescription
DEVICEOpti-Free RepleniSHCommercially available contact lens solution used for pre-soaking balafilcon A contact lenses overnight prior to lens insertion.
DEVICEReNu MultiPlusCommercially available contact lens solution used for pre-soaking balafilcon A contact lenses overnight prior to lens insertion.
DEVICEBalafilcon ACommercially available silicone hydrogel contact lenses removed from blister pack and soaked overnight in Opti-Free Replenish, ReNu MultiPlus, or Unisol 4, then applied to the eye and worn for 2 hours.
OTHERUnisol 4Commercially available non preserved sterile saline solution used for pre-soaking balafilcon A contact lenses overnight prior to lens insertion.

Timeline

Start date
2010-03-01
Primary completion
2010-09-01
Completion
2010-09-01
First posted
2010-04-09
Last updated
2012-10-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01100424. Inclusion in this directory is not an endorsement.