Clinical Trials Directory

Trials / Completed

CompletedNCT01959854

Efficacy of Topical 0.2% Xanthan Gum in Patients With Dry Eye

Evaluation of Xanthan Gum Eye Drops in Patients With Dry Eye

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
SIFI SpA · Industry
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the effect of an ophthalmic solution containing 0.2% xanthan gum in reducing symptoms and signs of dry eye as well as tear film markers of oxidative stress.

Detailed description

Oxidative stress is the result of an imbalance between the production of reactive oxygen species (ROS) and antioxidant systems . The eye is constantly exposed to solar UV radiation which is the major inducer of ROS production and therefore oxidative stress has been implicated in the pathogenesis of several eye disease, including dry eye. Xanthan gum is a complex exopolysaccharide utilized as a food additive. Its chemical structure shows a capacity to react with ROS indicating a role as an anti-oxidative molecule. In the present study aging patients with dry eye will be enrolled. Signs and symptoms of dry eye as well as levels of oxidative stress in tear will be evaluated afte 30 days of treatment with eye drops containing carboxymethylcellulose or xanthan gum.

Conditions

Interventions

TypeNameDescription
DEVICEcarboxymethylcellulose0.25% carboxymethylcellulose preservative free
DEVICExanthan gum0.2% xanthan gum preservative free

Timeline

Start date
2013-09-01
Primary completion
2014-10-01
Completion
2014-10-01
First posted
2013-10-10
Last updated
2014-10-16

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT01959854. Inclusion in this directory is not an endorsement.

Efficacy of Topical 0.2% Xanthan Gum in Patients With Dry Eye (NCT01959854) · Clinical Trials Directory