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Acute Comfort and Blur of Systane Ultra and Systane

NCT00748865 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2012-02-02

Study results available
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Summary

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

Conditions

  • Dry Eye

Interventions

OTHER

Systane Ultra Lubricant Eye Drops

Systane Ultra Lubricant Eye Drops 1 drop each eye one time

OTHER

Systane Lubricant Eye Drops

Systane Lubricant Eye Drops 1 drop each eye one time

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-07-31
Primary Completion
2008-08-31
Completion
2008-08-31

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 NCT00748865 on ClinicalTrials.gov