Trials / Terminated
TerminatedNCT04163328
Effects of Supplementation With PUFAs and Antioxidants for Contact Lens Discomfort
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 31 (actual)
- Sponsor
- University of Alabama at Birmingham · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
HydroEye® is a dietary omega 3 fatty acid supplement that contains both EPA and DHA, as well as GLA and ALA in the form of black currant seed oil. It also has vitamins A, E, C, B6, and magnesium, many of which are involved in fatty acid metabolism. In 2013, Sheppard et al. tested HydroEye® in dry eye patients who were not contact lens wearers and found that symptoms and corneal smoothness improved in response to HydroEye® supplementation. To date, HydroEye® has not been assessed in patients with contact lens discomfort; therefore, the purpose of this clinical trial is to determine the efficacy of HydroEye® as a treatment for contact lens discomfort.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | HydroEye® | This is an omega-3 fatty acids supplement. |
Timeline
- Start date
- 2022-09-16
- Primary completion
- 2024-08-21
- Completion
- 2024-08-21
- First posted
- 2019-11-14
- Last updated
- 2025-03-06
- Results posted
- 2025-03-06
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04163328. Inclusion in this directory is not an endorsement.