A 2-week Clinical Comparison of SYSTANE® Ultra to Sensitive Eyes Rewetting Drops in Contact Lens Wearing Patients.

NCT00769665 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 47

Last updated 2012-02-02

No results posted yet for this study

Summary

To evaluate safety with the use of Systane Ultra in contact lens wearers. A comparison to a currently marketed contact lens rewetting drop will be included as a control.

Conditions

  • Dry Eye

Interventions

OTHER

Systane Ultra

Re-wetting ocular eye drop

OTHER

Sensitive Eyes Rewetting Drops

Re-wetting ocular eye drop

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-10-31
Primary Completion
2009-01-31
Completion
2009-01-31

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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 NCT00769665 on ClinicalTrials.gov