Clinical Trials Directory

Trials / Completed

CompletedNCT00761202

Performance and Acceptance of Optive Versus Hylocomod Eyedrops in Patients With Dry Eye Symptoms

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

Summary

This study evaluates the performance and acceptance of Optive versus Hylocomod eyedrops, when administered for one month to patients with mild to moderate dry eye symptoms, with and without contact lenses.

Conditions

Interventions

TypeNameDescription
DRUGA sterile solution containing sodium carboxymethylcellulose and glycerin, preserved with PURITE®Eyedrops as required, but at least 3 times per day
DRUGSodium hyaluronateEyedrops as required, but at least 3 times per day

Timeline

Start date
2007-08-01
Primary completion
2008-06-01
Completion
2008-06-01
First posted
2008-09-29
Last updated
2013-11-19
Results posted
2010-02-04

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00761202. Inclusion in this directory is not an endorsement.

Performance and Acceptance of Optive Versus Hylocomod Eyedrops in Patients With Dry Eye Symptoms (NCT00761202) · Clinical Trials Directory