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

NCT01100424 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2012-10-23

No results posted yet for this study

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

  • Corneal Staining

Interventions

DEVICE

Opti-Free RepleniSH

Commercially available contact lens solution used for pre-soaking balafilcon A contact lenses overnight prior to lens insertion.

DEVICE

ReNu MultiPlus

Commercially available contact lens solution used for pre-soaking balafilcon A contact lenses overnight prior to lens insertion.

DEVICE

Balafilcon A

Commercially 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.

OTHER

Unisol 4

Commercially available non preserved sterile saline solution used for pre-soaking balafilcon A contact lenses overnight prior to lens insertion.

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Jami Kern · Alcon, Ltd.

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2010-09-30
Completion
2010-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01100424 on ClinicalTrials.gov