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Clinical Evaluation of the Causes of Contact Lens Related Dry Eye

NCT00995189 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 159

Last updated 2016-11-17

No results posted yet for this study

Summary

The purpose of this study was to clinically evaluate the potential causes of contact lens-related dry eye.

Conditions

  • Contact Lens Related Dry Eye

Interventions

DEVICE

Opti-Free RepleniSH

Contact lens care solution containing polyquaternium-1 (PQT)

DEVICE

ReNu MultiPlus

Contact lens care solution containing polyhexamethylene biguanide (PHMB)

DEVICE

Contact lenses

Daily wear, frequent replacement contact lenses per participant's habitual brand and power.

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2010-04-30
Completion
2010-04-30

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 NCT00995189 on ClinicalTrials.gov