Comparison of Frequency of Use of Optive and Systane

NCT00406510 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL

Last updated 2007-06-01

No results posted yet for this study

Summary

The purpose of this study is subjectively compare duration of action between Optive and Systane.

Conditions

  • Dry Eye

Interventions

DRUG

Optive, Systane

Sponsors & Collaborators

  • Innovative Medical

    lead INDUSTRY

Principal Investigators

  • Milton Hom, OD · Private Practice

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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 NCT00406510 on ClinicalTrials.gov