Trials / Completed
CompletedNCT02980913
Difference in the Frequency of Use of Lachrymal Substitutes in Patients With Moderate to Severe Dry Eye Syndrome
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 45 (actual)
- Sponsor
- Medical University of Vienna · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Dry eye syndrome is a highly prevalent ocular disease with an increasing incidence in the elderly population. Topically administered lubricants are the basis for treatment of this disease. Relief of symptoms in patients with moderate to severe dry eye disease is usually reached by the use of artificial tears during the day. Nighttime relief is often achieved by substances known to be more adhesive to the ocular surface, such as gels.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Thealoz Duo eye drops and Thealoz Duo gel | Thealoz Duo eye drops during the day + Thealoz Duo gel at night (1 drop before going to bed) for 7 days |
| DEVICE | Thealoz Duo gel | Thealoz Duo gel during the day and at night for 7 days |
Timeline
- Start date
- 2016-02-11
- Primary completion
- 2016-05-17
- Completion
- 2016-05-17
- First posted
- 2016-12-02
- Last updated
- 2019-08-22
Locations
1 site across 1 country: Austria
Source: ClinicalTrials.gov record NCT02980913. Inclusion in this directory is not an endorsement.