Clinical Trials Directory

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

TypeNameDescription
DRUGHydroEye®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

Source: ClinicalTrials.gov record NCT04163328. Inclusion in this directory is not an endorsement.

Effects of Supplementation With PUFAs and Antioxidants for Contact Lens Discomfort (NCT04163328) · Clinical Trials Directory