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Residence Time Evaluation of Systane Ultra Lubricant Eye Drops vs. Hialid and Saline

NCT01252121 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2012-10-30

No results posted yet for this study

Summary

The purpose of this study is to evaluate the ocular retention time of Systane Ultra compared to Hialid and saline.

Conditions

  • Dry Eye Syndrome

Interventions

OTHER

Systane Ultra Lubricant Eye Drops

One drop in study eye, one time, during office visit.

OTHER

Hialid 0.1 Artificial Tears Eye Drops

One drop in study eye, one time, during office visit.

OTHER

Unisol 4 Saline Solution

One drop in study eye, one time, during office visit.

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
2010-10-31
Primary Completion
2011-06-30
Completion
2011-06-30

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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 NCT01252121 on ClinicalTrials.gov