Acute Comfort and Haze Profile of FID 114657

NCT00983203 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2012-02-02

No results posted yet for this study

Summary

The purpose of this study is to describe the acute comfort and haze profile of FID 114657 in dry eye patients.

Conditions

  • Dry Eye

Interventions

OTHER

FID 114657 ORB Preserved Ocular Emulsion

1 drop OU

OTHER

Soothe XP Lubricant Eye Drops

1 drop OU

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2009-08-31

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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 NCT00983203 on ClinicalTrials.gov