Trials / Completed
CompletedNCT01742884
Efficacy and Safety of a Treatment for Dry Eye Syndrome: Thealoz
Evaluation of the Efficacy and Safety of a Treatment for Dry Eye Syndrome: Thealoz
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- Instituto Universitario de Oftalmobiología Aplicada (Institute of Applied Ophthalmobiology) - IOBA · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine if Thealoz is effective in Dry Eye Syndrome exposed to controlled adverse environmental conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Thealoz | Instillation of 1 drop of Thealoz |
| OTHER | Vehicle | 1 drop of the vehicle will be instillated in the eye |
Timeline
- Start date
- 2012-12-01
- Primary completion
- 2014-06-01
- Completion
- 2014-06-01
- First posted
- 2012-12-06
- Last updated
- 2015-01-08
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT01742884. Inclusion in this directory is not an endorsement.