MedTrace Logo

Evaluation of Contact Lenses and Conjunctival Staining in Normal Patients

NCT00799422 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26

Last updated 2012-11-16

Study results available
· View outcomes & findings →

Summary

The purpose of this study was to investigate contact lens fit, lens parameters, and conjunctival staining in a sample of subjects with various contact lens/solution combinations.

Conditions

  • Conjunctival Staining

Interventions

DEVICE

Complete Easy Rub

Commercially marketed contact lens solution for contact lens care

DEVICE

ReNu MultiPlus

Commercially marketed contact lens solution for contact lens care

DEVICE

Clear Care

Commercially marketed contact lens solution for contact lens care

DEVICE

Contact lenses

Acuvue Oasys silicone hydrogel contact lenses per participant's habitual prescription worn 8-10 hours per day for one week.

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Alison Ramsey, O.D. · Alcon Research

Study Design

Allocation
RANDOMIZED
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2009-03-31
Completion
2009-03-31

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 NCT00799422 on ClinicalTrials.gov