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Dry Eye Disease in the Vitamin D and Omega-3 Trial (VITAL)

Dry Eye Disease in the Vitamin D and Omega-3 Trial (VITAL)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01880463
Enrollment
25875
Registered
2013-06-19
Start date
2010-07-31
Completion date
2021-12-31
Last updated
2019-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dry Eye Disease

Keywords

Dry eye disease, incidence, progression

Brief summary

The VITamin D and OmegA-3 Trial (VITAL; NCT 01169259) is a randomized clinical trial in 25,875 U.S. men and women investigating whether taking daily dietary supplements of vitamin D3 (2000 IU) or omega-3 fatty acids (Omacor fish oil, 1 gram) reduces the risk of developing cancer, heart disease, and stroke in people who do not have a prior history of these illnesses. This ancillary study is being conducted among participants in VITAL and will examine whether omega-3 fatty acids or vitamin D3, compared to placebo, reduce the incidence and/or progression of dry eye disease.

Detailed description

This ancillary study to VITAL will examine the efficacy of omega-3 fatty acids and vitamin D3 in prevention of dry eye disease. The primary aims are to test whether omega-3 fatty acid supplementation (1) reduces the incidence of dry eye disease, and (2) improves the natural history of dry eye disease by relieving symptoms and other impacts on quality of life. Secondary aims are to estimate the incidence of dry eye disease in the US, prospectively examine the natural history of dry disease, explore factors that could modify or influence the impact of omega-3 fatty acid supplementation, evaluate the interrelationship of dry eye disease and depression, and test for possible independent or joint effects of vitamin D3 supplementation in the incidence and natural history of dry eye disease.

Interventions

DIETARY_SUPPLEMENTVitamin D3
DIETARY_SUPPLEMENTVitamin D3 placebo

Sponsors

National Eye Institute (NEI)
CollaboratorNIH
Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* All participants in VITAL (NCT 01169259) are eligible to participate in this ancillary study.

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Dry Eye Disease5 yearsReport of a diagnosis of dry eye disease confirmed by medical record review.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026