Clinical Trials Directory

Trials / Completed

CompletedNCT01311609

A Multi-Site Post Marketing Surveillance Study for Systane in Indian Patients

Multi-Site Post Marketing Surveillance Study for Systane in Indian Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
300 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is a multi-site, unmasked PMS Study. The purpose of the study is to evaluate the physical effects of Systane Lubricant Eye Drops.

Detailed description

This study is a multi-site, unmasked PMS Study. The purpose of the study is to evaluate the physical effects of Systane Lubricant Eye Drops. The assessed effects include: corneal and conjunctival staining, and ocular signs and symptoms. This is a two week prospective study.

Conditions

Interventions

TypeNameDescription
OTHERSystaneSystane Lubricant Eye Drops \[1-2 Drops in each eye four times daily (QID)\]

Timeline

Start date
2010-11-01
Primary completion
2011-07-01
Completion
2011-07-01
First posted
2011-03-09
Last updated
2012-02-02

Source: ClinicalTrials.gov record NCT01311609. Inclusion in this directory is not an endorsement.