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Evaluate Artificial Tear Efficacy in Moderate to Severe Dry Eye

NCT00724412 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 279

Last updated 2012-02-02

No results posted yet for this study

Summary

Comparison of two Dry Eye products

Conditions

  • Dry Eye

Interventions

OTHER

Systane

Dry Eye relief eye drops

OTHER

Optive

Dry Eye relief eye drops

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2009-02-28
Completion
2009-02-28

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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 NCT00724412 on ClinicalTrials.gov