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Omega-3 Fatty Acid Supplement
EPA + DHA Ruby-O for Bioavailability
N/A
Waitlist Available
Research Sponsored by Midwest Center for Metabolic and Cardiovascular Research
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to 24 hours
Awards & highlights
Study Summary
This trial will compare the absorption of EPA and DHA from two different supplements in healthy adults.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline to 24 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to 24 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Baseline-adjusted geometric mean ratio for EPA + DHA AUC
Secondary outcome measures
Baseline-adjusted AUC for EPA and DHA
Baseline-adjusted maximum concentration for EPA, DHA, and EPA + DHA
Baseline-adjusted, dose-normalized AUC for EPA, DHA, and EPA + DHA
+4 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: EPA + DHA Ruby-OExperimental Treatment1 Intervention
Subject will receive a single 1000 mg oral dose of EPA + DHA Ruby-O capsule
Group II: EPA + DHA Krill OilActive Control1 Intervention
Subject will receive a single 1000 mg oral dose of EPA + DHA krill oil capsule
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
EPA + DHA Ruby-O
2022
N/A
~30
Find a Location
Who is running the clinical trial?
Midwest Center for Metabolic and Cardiovascular ResearchLead Sponsor
20 Previous Clinical Trials
824 Total Patients Enrolled
2 Trials studying Bioavailability
48 Patients Enrolled for Bioavailability
NaturmegaUNKNOWN
Kevin C Maki, PhDStudy DirectorMB Clinical Research & Consulting
16 Previous Clinical Trials
936 Total Patients Enrolled
2 Trials studying Bioavailability
48 Patients Enrolled for Bioavailability
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