Acute Comfort of Lubricant Eye Drop FID 111421

NCT00673959 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2012-02-02

Study results available
· View outcomes & findings →

Summary

To evaluate the acute comfort and blurring profile between two artificial tears products in dry eye patients

Conditions

  • Dry Eye

Interventions

OTHER

Lubricant Eye Drop FID 111421

Lubricant Eye Drop FID 111421 1 drop each eye one time

OTHER

Optive Lubricant Eye Drop

Optive Lubricant Eye Drop 1 drop each eye one time

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2008-02-29

More Related Trials

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 NCT00673959 on ClinicalTrials.gov