Clinical Trials Directory

Trials / Completed

CompletedNCT01030237

An Evaluation of the Safety and Efficacy of FID 114657

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
153 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety and efficacy of FID 114657 in comparison to Soothe XP in a specified population of dry eye patients.

Conditions

Interventions

TypeNameDescription
OTHERFID 1146571 drop both eyes four times a day for 6 weeks
OTHERSoothe XP Lubricant Eye Drops1 drop both eyes four times a day for 6 weeks

Timeline

Start date
2009-11-01
Primary completion
2010-01-01
First posted
2009-12-11
Last updated
2012-02-02

Source: ClinicalTrials.gov record NCT01030237. Inclusion in this directory is not an endorsement.