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NCT05763940

Efficacy of OmegaBoost to Increase Omega-3 Levels in Healthy Individuals

Active, enrolled NA Last updated 24 April 2024
What this trial tests

NA trial testing OmegaBoost in Dry Eye Syndromes in 130 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
25 May 2022
Primary endpoint
25 May 2024
25 June 2024

Quick facts

Lead sponsorWestern University of Health Sciences
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment130
Start date25 May 2022
Primary completion25 May 2024
Estimated completion25 June 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Western University of Health Sciences

Who can join

18 and older, any sex, with Dry Eye Syndromes or Age-Related Macular Degeneration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine increases in the Omega Index test indicating optimal Omega-3s particularly eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) levels for overall systemic benefits including healthy cardiovascular health and cholesterol levels as shown in the OmegaIndex (OmegaQuant) research.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Dry Eye Syndromes

Currently open trials in the same condition.

Other Western University of Health Sciences trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05763940.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing