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Evaluation of the Safety and Biologic Effects of an Eicosapentaenoic (EPA)-Enriched Oil (EPA)

Primary Purpose

Heart Disease

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
EPA 600
EPA 1800
Olive Oil
DHA
Sponsored by
Cardiovascular Research Associates
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Disease focused on measuring Heart Disease Risk Reduction

Eligibility Criteria

21 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • healthy male or surgically sterile females between ages 21-70.
  • BMI of 20-35.

Exclusion Criteria:

  • competitive exerciser.
  • current smokers.
  • those already taking dietary supplements (EPA, DHA, flax seed oil, fish oil, cod liver oil, weight control products, or high doses of vitamin C (> 500 mg/day) or vitamin E (> 400 units/day).
  • those consuming more than 3 oily fish species/week.
  • those consuming > 2 drinks/day.
  • those with a history of a bleeding disorder, or history of significant cardiac, renal, hepatic, gastro-intestinal, pulmonary, neoplastic, biliary or endocrine disorders such as uncontrolled thyroid disease, or uncontrolled hypertension or diabetes.
  • those taking medications affecting serum lipids, body weight, or blood clotting.

Sites / Locations

  • Cardiovascular Research Associates

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Olive Oil

EPA 1800

DHA

EPA 600

Arm Description

Olive Oil 600 mg/day

1800 mg/day

DHA 600 mg/day

EPA 600 mg/day

Outcomes

Primary Outcome Measures

No change in safety laboratory tests including comprehensive metabolic profile and complete blood count.

Secondary Outcome Measures

Efficacy will be assessed by measuring changes in fatty acid profile and or fatty acid ratios.

Full Information

First Posted
September 30, 2009
Last Updated
June 22, 2011
Sponsor
Cardiovascular Research Associates
Collaborators
Dupont Applied Biosciences
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1. Study Identification

Unique Protocol Identification Number
NCT00988585
Brief Title
Evaluation of the Safety and Biologic Effects of an Eicosapentaenoic (EPA)-Enriched Oil
Acronym
EPA
Official Title
Evaluation of the Safety and Biologic Effects of an Eicosapentaenoic (EPA)-Enriched Oil
Study Type
Interventional

2. Study Status

Record Verification Date
June 2011
Overall Recruitment Status
Completed
Study Start Date
April 2009 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Cardiovascular Research Associates
Collaborators
Dupont Applied Biosciences

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal is to test the safety and efficacy of an EPA-enriched oil made by DuPont. DuPont wishes to corroborate the safety of its novel oil rich in EPA in humans prior to placing such a dietary supplement on the market. The goal of this study is to test this oil at doses of 600 mg and 1800 mg of EPA/day as compared to olive oil placebo and a comparator oil providing 600 mg of DHA/day over a 6 wk period. In a parallel arm study design, 120 healthy adults will be randomized to one of four groups (30 in each group) and studied in both the fasting and post-prandial state.
Detailed Description
The safety profile of omega-3 fatty acids is considered to be excellent, and has been recognized as safe (GRAS) by the US Food and Drug Administration when EPA and DHA (docosahexanoic acid) are given together at a dose of 3 grams/day or less. Safety will be monitored by assessing for adverse reactions, measuring vital signs and a variety of laboratory tests including a complete metabolic profile and complete blood count. Efficacy will be assessed by measuring changes in fatty acid profile and or fatty acid ratios. The goal of this study is to test this EPA oil at doses of 600 mg and 1800 mg of EPA/day as compared to olive oil placebo and a comparator oil providing 600 mg of DHA/day over a 6 wk period. In a parallel arm study design, 120 healthy adults will be randomized to one of four groups (30 in each group) and studied in both the fasting and post-prandial state.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Disease
Keywords
Heart Disease Risk Reduction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Olive Oil
Arm Type
Placebo Comparator
Arm Description
Olive Oil 600 mg/day
Arm Title
EPA 1800
Arm Type
Active Comparator
Arm Description
1800 mg/day
Arm Title
DHA
Arm Type
Active Comparator
Arm Description
DHA 600 mg/day
Arm Title
EPA 600
Arm Type
Active Comparator
Arm Description
EPA 600 mg/day
Intervention Type
Dietary Supplement
Intervention Name(s)
EPA 600
Other Intervention Name(s)
omega 3 fat, fish oil
Intervention Description
EPA 600 mg/day for 6 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
EPA 1800
Other Intervention Name(s)
omega 3 fat, fish oil
Intervention Description
1800 mg/day for 6 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
Olive Oil
Other Intervention Name(s)
Oleic acid
Intervention Description
600 mg/day for 6 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
DHA
Other Intervention Name(s)
omega 3 fat, fish oil
Intervention Description
600 mg/day for 6 weeks
Primary Outcome Measure Information:
Title
No change in safety laboratory tests including comprehensive metabolic profile and complete blood count.
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Efficacy will be assessed by measuring changes in fatty acid profile and or fatty acid ratios.
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: healthy male or surgically sterile females between ages 21-70. BMI of 20-35. Exclusion Criteria: competitive exerciser. current smokers. those already taking dietary supplements (EPA, DHA, flax seed oil, fish oil, cod liver oil, weight control products, or high doses of vitamin C (> 500 mg/day) or vitamin E (> 400 units/day). those consuming more than 3 oily fish species/week. those consuming > 2 drinks/day. those with a history of a bleeding disorder, or history of significant cardiac, renal, hepatic, gastro-intestinal, pulmonary, neoplastic, biliary or endocrine disorders such as uncontrolled thyroid disease, or uncontrolled hypertension or diabetes. those taking medications affecting serum lipids, body weight, or blood clotting.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael L Dansiner, M.D.
Organizational Affiliation
Cardiovascular Research Associates
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cardiovascular Research Associates
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Evaluation of the Safety and Biologic Effects of an Eicosapentaenoic (EPA)-Enriched Oil

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