Trials / Completed
CompletedNCT06517667
Efficacy and Safety of Different Hyaluronic Acid Tear Substitutes Formulations in Evaporative Dry Eye
Efficacy and Safety of Different Hyaluronic Acid Tear Substitutes Formulations in Evaporative Dry Eye: A Randomized, Single-Blind, Comparative Study
- Status
- Completed
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- University of Seville · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The objective of the study is to compare the efficacy and safety of different hyaluronic acid tear substitutes formulations in patients with evaporative dry eye. For this purpose, a randomized, single-blind clinical trial has been designed.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Icross tear substitute | Patients were instructed to instill 1 drop of 0.20% Cross-linked hyaluronic acid substitute into each eye 3 times per day for 3 months. |
| DRUG | Hyabak tear substitute | Patients were instructed to instill 1 drop of 0.15% hyaluronic acid substitute into each eye 3 times per day for 3 months. |
Timeline
- Start date
- 2023-11-01
- Primary completion
- 2024-02-01
- Completion
- 2024-06-01
- First posted
- 2024-07-24
- Last updated
- 2024-07-26
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT06517667. Inclusion in this directory is not an endorsement.