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Omega 3 IndexNCT07900425

A Randomized, Double-blind, Placebo Controlled, Parallel Virtual Clinical Trial to Investigate the Efficacy of Marine Oil Products on Omega-3 Status in Healthy Adults

A study testing Omega-3 Softgel, Ultimate Omega Softgel and Ultimate Omega 2X Softgel in people with Omega 3 Index and Nutrient Status, run by Nordic Naturals at 1 site in Canada.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

Heart disease is the leading cause of death worldwide. The Omega-3 Index (O3I) is a blood test that measures the amount of the omega-3 fats EPA and DHA in red blood cells. Research suggests that people with an O3I above 8% have a lower risk of dying from coronary heart disease than people with an O3I below 4%. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Omega-3 Softgel, Ultimate Omega Softgel and Ultimate Omega 2X Softgel
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
600 participants
Where
1 siteCanada
Study dates
26 Oct 2026to 1 Dec 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Males and females 18 years and older
  • Females not of child-bearing potential, defined as those who have undergone a sterilization procedure (e.g. hysterectomy, bilateral oophorectomy, bilateral tubal ligation, complete endometrial ablation) or have been post-menopausal for at least 1 year prior to screening Or,
  • Individuals of child-bearing potential must self-report that they are not pregnant and agree to use a medically approved method of birth control for the duration of the study. All hormonal birth control must have been in use for a minimum of three months. Acceptable methods of birth control include:
  • Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo-Provera, Lunelle), or hormone implant (Norplant System)
  • Double-barrier method
  • Intrauterine devices
Show all 35Show fewer
  • Non-heterosexual lifestyle and agrees to use contraception if planning on changing to heterosexual partner(s)
  • Vasectomy of partner at least 6 months prior to screening
  • Abstinence and agrees to use contraception if planning on becoming sexually active during the study 3. Normal diet includes low fatty fish intake (≤4 servings per month) 4. Agrees to avoid consuming foods and beverages fortified with omega-3 fatty acids for the study duration 5. Agrees to maintain current lifestyle habits (diet, physical activity, medications, supplements, and sleep) as much as possible throughout the study 6. Provided voluntary, written, informed consent to participate in the study 7. Willing and able to consume study product and complete all questionnaires, diaries, and assessments required for participation 8. Healthy as determined by medical history and no unstable diagnosed medical conditions 7.2 Exclusion Criteria
  • Individuals who self-report as being pregnant, breast feeding, or planning to become pregnant during the study
  • Self-reported allergy, sensitivity, intolerance, or dietary restriction preventing consumption of investigational product or placebo ingredients
  • Self-reported allergy to marine foods and/or by-products (e.g, fish, shellfish, or seafood)
  • Self-reported current use of omega-3 supplements (see Section 7.3.2)
  • Self-reported ongoing and unstable diseases/conditions in the past six months, including:
  • Gastrointestinal diseases
  • Hypertension
  • Type I or type II diabetes
  • Cardiovascular disease
  • Kidney and/or liver diseases
  • Thyroid condition
  • Autoimmune disease or immune compromised
  • Self-reported confirmation of any significant psychological condition/disorders
  • Self-reported major surgery in the past 3 months or individuals who have planned surgery during the course of the study
  • Self-reported cancer, except skin basal cell carcinoma completely excised with no chemotherapy or radiation with a follow up that is negative. Volunteers with cancer in full remission for more than five years after diagnosis are acceptable
  • Self-reported confirmation of blood/bleeding disorders
  • Self-reported confirmation of a HIV-, Hepatitis B- and/or C-positive diagnosis
  • Self-reported alcohol intake average of >2 standard drinks per day
  • Self-reported alcohol or drug abuse within the last 12 months that has required treatment
  • Self-reported use of cannabinoid products of >2 times per week
  • Self-reported current use of prescribed and/or OTC medications/supplements that may impact the efficacy and/or safety of the investigational product (Sections 7.3.1 and 7.3.2)
  • Participation in other clinical research studies 30 days prior to randomization
  • Individuals who are unable to give informed consent
  • Any other condition or lifestyle factor that may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant 7.3 Concomitant Medications Participants who are taking any prescribed medications that are considered not to affect the study outcomes must agree to maintain their current dosing regimen during the study unless otherwise recommended by their general practitioner/nurse practitioner.
  • 7.3.1 Prescribed Medications Not applicable. 7.3.2 Over-the-counter Medications, Supplements, and Food/Drinks Participants who are currently consuming the following OTC medications, supplement and food/drinks will not be allowed to participate..
  • 1. Omega-3 supplements

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Canada1 site, 1 recruiting
  • KGK Science Inc

    London, Ontario, N6B 3L1

    Erin Lewis, PhD, (519) 438-9374, elewis@kgkscience.com

    Rishu Srivastava, (519) 438-9374, rsrivastava@kgkscience.com

    Recruiting

Other trials in Canada

About this study

Heart disease is the leading cause of death worldwide. The Omega-3 Index (O3I) is a blood test that measures the amount of the omega-3 fats EPA and DHA in red blood cells. Research suggests that people with an O3I above 8% have a lower risk of dying from coronary heart disease than people with an O3I below 4%.

Eating fatty fish two or more times per week may help improve omega-3 status, but many people do not eat enough fish because of taste preferences or concerns about contaminants. Omega-3 supplements, such as fish oil and algae oil, can provide EPA and DHA directly and may help raise the Omega-3 Index. Research suggests that algae oil can be as effective as fish oil for increasing EPA and DHA levels.

This study will evaluate whether different fish-oil and algae-oil products-including softgels, liquids, and gummies-improve omega-3 status in healthy adults who eat little fatty fish. Participants will be asked to keep their usual diet, activity, medications, supplements, and lifestyle habits as consistent as possible during the study.

Read the detailed description

Cardiovascular diseases are the leading cause of mortality and a major contributor of disability worldwide, with approximately 18.6 million deaths reported in 2021 (1). Early identification of at-risk individuals allows for an opportunity to administer prevention strategies in order to help support longevity and mitigate the progression of disease. In 2004, Omega-3 Index (O3I) was identified as a biomarker for the risk of death from coronary heart disease (2). This indicator of omega-3 status is defined as the combined percentage of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) of total fatty acids in red blood cell membranes. Maintaining an O3I of above 8% has been linked to a lower risk of coronary heart disease (3). Using pooled data from 27,000 participants across 10 studies, a 35% lower risk of mortality from coronary heart disease was reported among those with an O3I of above 8%, compared to those with an O3I of below 4% (3).

Reaching an O3I of above 8% may be attainable with more than two servings of fatty fish each week (4-6), aligning with national dietary recommendations. Dietary Guidelines for Americans recommend fish and seafood intake at least 2 to 3 times per week (7). The previous 2007 Canada's Food Guide recommended at least two servings of fish per week (8), of which was updated to include seafood an example of a healthy protein food source without defining specific amounts (9). However, it is recognized that most individuals fall short of adequate intake leading to a high prevalence of suboptimal O3I and increased risk of chronic disease (10). According to national survey data (Canadian Community Health Survey 2004 and 2015, Nutrition), approximately one in six Canadians reported daily seafood consumption (11), with a similar percentage reported in the United States based on the National Health and Nutrition Examination Survey 2007-2008 and 2015-2016 (12). Despite it being widely known that diet is major contributor of supporting and maintaining overall health, the lack of variation in foods rich in EPA and DHA makes it challenging to overcome personal tastes and preferences (e.g., smells and texture). Additionally, concerns for mercury or environmental toxins in certain fish contributes to lower intakes (13). Thus, improving and maintaining O3I with only foods may not be feasible and cross-sectional studies have shown that the odds of having an O3I above 8% was greatest among those with 3 or more serving of fish per week along with supplementation (6,14). With direct supply of EPA and DHA, marine-derived supplements continue to be a promising strategy for augmenting the diet to promote a range of health benefits.

The investigational products (IP) used in the current study are animal- (e.g., fish oil) and plant-based (e.g., algae oil) marine oil products of varying doses and forms (softgel, liquid, and gummy). In a recent randomized, double-blind, placebo-controlled, parallel clinical trial, the bioavailability of EPA and DHA from algal (1:3) and fish oil (3:2) supplementation were compared in healthy adults aged 21 to 82 at six and 14 weeks (15). Results demonstrated no statistical difference in plasma DHA and EPA bioavailability between the products (15), suggesting the use of algae oil as a sufficient source of EPA and DHA. Independent of the wide variation in dose, intervention period, and study population in this research field, EPA and DHA supplementation is linked to an improvement in O3I (16). However, further investigation is needed to determine the influence of commercially available marine oil products on omega-3 status to support its use for eliciting a O3I response. In a previous randomized, placebo-controlled, double-blind, parallel trial, 115 healthy men and women were provided one of five doses of marine-derived supplements for approximately five months (17). Findings showed a dose-dependent response of O3I (17). However, authors suggested the need for understanding how different ratios of EPA and DHA can influence O3I response.

The objective of this current study is to investigate the efficacy of marine oil products on omega-3 status in healthy adults. Part 1 will consist of softgel study products and Part 2 will consist of liquid, gummy chew and comparator study products. The study will enroll healthy adults aged 18 years or older with low fatty fish intake (< 4 servings per month). All participants will be required to agree to maintain their current lifestyle habits, including but not limited to diet, physical activity, medications, supplements, and sleep as much as possible throughout the study. Furthermore, participants must be willing to complete all questionnaires, diaries, and assessments, as well as self-report the ability to consume the investigational product. Those with self-confirmed history or current diagnosis of any significant disease of the gastrointestinal tract, or other ongoing and unstable diseases/conditions in the past six months will be excluded. Use of prescribed and/or over-the-counter (OTC) medications, supplements, and/or consumption of food/drinks that may impact the efficacy and/or safety of the investigational product will be prohibited to reduce any confounding effects on study outcomes and ensure the safety of the enrolled study population.

Being tested
Omega-3 Softgel, Ultimate Omega Softgel, Ultimate Omega 2X Softgel, Ultimate Omega One Daily Softgel, Ultimate Omega Plant-Based Softgel
Keywords
Omega-3, Omega-3 index, Supplements, Fish oil, Algae oil, Healthy adults

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Omega-3 SoftgelDietary supplement

    Omega-3 Softgel

  • Ultimate Omega SoftgelDietary supplement

    Ultimate Omega Softgel

  • Ultimate Omega 2X SoftgelDietary supplement

    Ultimate Omega 2X Softgel

  • Ultimate Omega One Daily SoftgelDietary supplement

    Ultimate Omega One Daily Softgel

  • Ultimate Omega Plant-Based SoftgelDietary supplement

    Ultimate Omega Plant-Based Softgel

  • Ultimate Omega LiquidDietary supplement

    Ultimate Omega Liquid

  • Omega-3 LiquidDietary supplement

    Omega-3 Liquid

  • RO SEDietary supplement

    RO SE

  • placebo softgelDietary supplement

    placebo softgel

  • Placebo LiquidDietary supplement

    Placebo Liquid

  • Ultimate Omega MiniDietary supplement

    Ultimate Omega Mini

  • Ultimate Omega Gummy ChewDietary supplement

    Ultimate Omega Gummy Chew

Study groups in NCT07900425
Study groupRoleWhat they receive
Placebo SoftgelPlacebo comparatorPlacebo softgel
Receives: Dietary Supplement: placebo softgel
Placebo LiquidPlacebo comparatorPlacebo liquid
Receives: Dietary Supplement: Placebo Liquid
Ultimate Omega SoftgelExperimentalUltimate Omega Softgel
Receives: Dietary Supplement: Ultimate Omega Softgel
Omega-3 LiquidExperimentalOmega-3 Liquid
Receives: Dietary Supplement: Omega-3 Liquid
Omega-3 SoftgelExperimentalOmega-3 Softgel
Receives: Dietary Supplement: Omega-3 Softgel
Ultimate Omega Mini SoftgelExperimentalUltimate Omega Mini Softgel
Receives: Dietary Supplement: Ultimate Omega Mini
Ultimate Omega One Daily SoftgelExperimentalUltimate Omega One Daily Softgel
Receives: Dietary Supplement: Ultimate Omega One Daily Softgel
Ultimate Omega Plant-Based SoftgelExperimentalUltimate Omega Plant-Based Softgel
Receives: Dietary Supplement: Ultimate Omega Plant-Based Softgel
RO SE SoftgelExperimentalRO SE Softgel
Receives: Dietary Supplement: RO SE
Ultimate Omega 2X SoftgelExperimentalUltimate Omega 2X Softgel
Receives: Dietary Supplement: Ultimate Omega 2X Softgel
Ultimate Omega LiquidExperimentalUltimate Omega Liquid
Receives: Dietary Supplement: Ultimate Omega Liquid
Ultimate Omega Gummy ChewExperimentalUltimate Omega Gummy Chew
Receives: Dietary Supplement: Ultimate Omega Gummy Chew

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Omega-3 Index

    Nutrient status of omega-3

    Measured: 3 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Oct 2026
  2. Study start26 Oct 2026 (estimated)
  3. Primary completion26 Oct 2027 (estimated)
  4. Study completion1 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
600 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07900425
Sponsor's protocol ID
25NNKGC01
Status last verified
Oct 2026
First submitted
21 Oct 2026
Last updated
28 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Need to ensure proprietary nature of the data. Anonymized data may be shared.

Publications

  • 1. Institute for Health Metrics and Evaluation (IHME). GBD Compare Data Visualization [Internet]. Seattle, WA: IHME, University of Washington; 2020. Available from: http:// vizhub.healthdata.org/gbdcompare 2. Harris WS, Von Schacky C. The Omega-3 Index: a new risk factor for death from coronary heart disease? Preventive Medicine. 2004 Jul;39(1):212-20. doi:10.1016/j.ypmed.2004.02.030 3. Harris WS, Del Gobbo L, Tintle NL. The Omega-3 Index and relative risk for coronary heart disease mortality: Estimation from 10 cohort studies. Atherosclerosis. 2017 Jul;262:51-4. doi:10.1016/j.atherosclerosis.2017.05.007 4. Lichtenstein AH, Appel LJ, Brands M, Carnethon M, Daniels S, Franch HA, et al. Diet and lifestyle recommendations revision 2006: A scientific statement from the American Heart Association Nutrition Committee. Circulation. 2006 Jul 4;114(1):82-96. doi:10.1161/CIRCULATIONAHA.106.176158 5. Gidding SS, Lichtenstein AH, Faith MS, Karpyn A, Mennella JA, Popkin B, et al. Implementing American Heart Association Pediatric and Adult Nutrition Guidelines: A scientific statement from the American Heart Association Nutrition Committee of the Council on Nutrition, Physical Activity and Metabolism, Council on Cardiovascular Disease in the Young, Council on Arteriosclerosis, Thrombosis and Vascular Biology, Council on Cardiovascular Nursing, Council on Epidemiology and Prevention, and Council for High Blood Pressure Research. Circulation. 2009 Mar 3;119(8):1161-75. doi:10.1161/CIRCULATIONAHA.109.191856 6. Jackson KH, Polreis JM, Tintle NL, Kris-Etherton PM, Harris WS. Association of reported fish intake and supplementation status with the omega-3 index. Prostaglandins, Leukotrienes and Essential Fatty Acids. 2019 Mar;142:4-10. doi:10.1016/j.plefa.2019.01.002 7. U.S. Department of Agriculture and U.S. Department of Health and Human Services. Dietary Guidelines for Americans, 2020-2025 [Internet]. Available from: https://www.dietaryguidelines.gov/ 8. Health Canada. Eating Well wit

Questions about this trial

What is this clinical trial studying?

A study testing Omega-3 Softgel, Ultimate Omega Softgel and Ultimate Omega 2X Softgel in people with Omega 3 Index and Nutrient Status, run by Nordic Naturals at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 35 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 28 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Omega-3 Index (time frame: 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07900425, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Oct 2026.

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