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Completed

NCT Number: NCT01415388

Study to Investigate the Effects of 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.

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Key information

Conditions

Age range

21 year–79 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cetero Research, Saint Charles, Missouri, United States

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Krill oil

Dietary Supplement

4 Capsules twice daily providing 0 (placebo), 0.5, 1.0, 2.0, or 4.0 g krill oil/day for a period of 12 weeks

Other names: Superba(TM) Krill Oil

Primary outcomes

  1. Change in fasting serum triglycerides

    Time frame: Baseline (Day 1) and at Day 85

Secondary outcomes

  1. Omega-3 index

    Time frame: At Days 1, 42, and 85

Sponsors and collaborators

Lead sponsor

Aker BioMarine Human Ingredients AS

Industry

Registry information

Official study title

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

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Aug 12, 2011
Registry last updated
Feb 21, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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