MedTrace Logo

The Physiological Consequence of Silicone-hydrogel Care-solution Bio-incompatibility

NCT00829751 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26

Last updated 2013-06-04

No results posted yet for this study

Summary

The purpose of this study is to more objectively evaluate potential lens-material/care solution bio-incompatibilities. We will do this by measuring corneal staining and the amount of fluorescein dye diffusion into the eye.

Conditions

  • Contact Lens Solution Toxicity

Interventions

DEVICE

PureVision lenses soaked in ReNu Multiplus

Purevision silicone hydrogel lenses

DEVICE

PureVision lenses soaked in OptiFree RePlenish

Purevision silicone hydrogel lenses soaked in OptiFree RePlenish

Sponsors & Collaborators

  • Alcon Research

    collaborator INDUSTRY

  • Southern California College of Optometry at Marshall B. Ketchum University

    lead OTHER

Principal Investigators

  • Jerry R Paugh, OD, PhD · Southern California College of Optometry at Marshall B. Ketchum University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • United States

Study Locations

More Related Trials

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 NCT00829751 on ClinicalTrials.gov