Trials / Completed
CompletedNCT05056233
Systane Hydration in Subjects Undergoing Cataract Surgery
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 35 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective of this study is to demonstrate reduced corneal staining with use of Systane Hydration among subjects with dry eye disease (DED) undergoing routine cataract removal and monofocal intraocular lens (IOL) implantation.
Detailed description
Subjects will attend 6 scheduled study visits for an individual duration of participation of 6 weeks. One eye (study eye) will be followed.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Systane Hydration lubricant eye drops | Sterile solution indicated for the temporary relief of burning and irritation due to dryness of the eye |
Timeline
- Start date
- 2022-01-18
- Primary completion
- 2023-01-12
- Completion
- 2023-01-12
- First posted
- 2021-09-24
- Last updated
- 2023-02-22
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT05056233. Inclusion in this directory is not an endorsement.