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
| Type | Name | Description |
|---|---|---|
| DEVICE | carboxymethylcellulose | 0.25% carboxymethylcellulose preservative free |
| DEVICE | xanthan gum | 0.2% 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.