Study to Investigate the Effects of Krill Oil on Fasting Serum Triglycerides



Status:Completed
Conditions:Healthy Studies
Therapuetic Areas:Other
Healthy:No
Age Range:Any
Updated:2/4/2013
Start Date:August 2011
End Date:December 2011
Contact:Ellen Myers
Email:ellen.myers@cetero.com
Phone:636-757-7081

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A Double-blind, Randomized, Multi-centre, Placebo-controlled Study to Investigate the Effects of Superba(TM) Krill Oil on Fasting Serum Triglycerides


The purpose of this study is to assess the effect of 12 weeks of daily supplementation with
Superba(TM) Krill Oil on fasting serum triglyceride levels and omega-3 index in subjects
whose habitual fatty fish and seafood intake is low and who have borderline high or high
fasting serum triglyceride levels.


Inclusion Criteria(not limited to):

- General good health with no existing co-morbidities

- Body mass index (BMI) less than 35 kg/m²

- Borderline high or high fasting serum triglycerides

- Clinically normal findings for hematology, clinical chemistry, and urinalysis

- Be willing to maintain dietary habits and physical activity levels throughout the
trial period (next 4 months)

- Have a low habitual consumption of fatty fish and seafood, defined as a frequency of
twice per month or less

Exclusion Criteria (not limited to):

- Familial hypercholesterolemia or severely high total cholesterol levels

- History or presence of significant cardiovascular disease or co-morbidities

- Known allergy to crustaceans (shellfish)

- Bleeding disorders

- Disturbed absorption due to changes in the gastrointestinal tract

- Participation in a clinical trial with an investigational product within 30 days
before screening

- Present or recent use (within 3 months of screening or the first screening visit, if
applicable) of any medication which is a known lipid modifying agent or any dietary
supplements that affect the level of blood cholesterol and triglycerides

- Current or recent diet, which in the opinion of the Investigator, deviates from a
normal diet (e.g., vegetarians may be acceptable, vegans are not acceptable)

- Female patients that are pregnant or nursing or females of childbearing potential who
are not on a method of birth control acceptable to the Investigator during treatment

- Patients with known coagulopathy or receiving anticoagulant therapy or co-morbidity
that would interfere with the study results

- Frequency of fatty fish and/or seafood consumption is greater than twice per month

- Present or recent use of any long-chain omega-3 fatty acid supplement

- Peri-menopausal women or post-menopausal women taking hormone replacement therapy

- Patients who test positive for human immunodeficiency virus (HIV) or hepatitis B or C

- Systolic blood pressure greater than 159 mmHg or diastolic blood pressure greater
than 99 mmHg or use of anti-hypertensive medication

- Diabetic subjects

- Staff of Cetero Research
We found this trial at
2
sites
St. Charles, Missouri 63301
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St. Charles, MO
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Fargo, North Dakota 58104
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Fargo, ND
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