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Acute Comfort and Blur of Systane and Optive

NCT00568386 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2012-02-02

Study results available
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Summary

To evaluate drop comfort, acceptability, preference and blur profile between two marketed artificial tears in both dry eye and non-dry eye patient population.

Conditions

  • Dry Eye

Interventions

OTHER

Systane Lubricant Eye Drops

Systane Lubricant Eye Drops 1 drop each eye once time

OTHER

Optive Lubricant Eye Drops

Optive Lubricant Eye Drops 1 drop each eye one time

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Mike Christensen · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-11-30
Completion
2007-12-31

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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 NCT00568386 on ClinicalTrials.gov