Seaweed Extract Supplementation and Metabolic Biomarkers

Sponsor
BioAtlantis Ltd. (Industry)
Overall Status
Completed
CT.gov ID
NCT03853343
Collaborator
University of Roehampton (Other)
10
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2
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Study Details

Study Description

Brief Summary

Double blinded, randomized, placebo controlled preliminary pilot exploratory investigation into the effects of brown seaweed extract supplementation, on fasting blood Insulin, fasting blood glucose, insulin sensitivity, blood inflammatory markers and tolerance in healthy overweight adults.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Seaweed extract
  • Dietary Supplement: Placebo
N/A

Detailed Description

Diabetes melitus is a group of metabolic disorders resulting from a defect in insulin production and/or insulin action. The World Health Organisation (WHO) has estimated that the total number of people with diabetes mellitus worldwide will increase from 171 million in 2000 to nearly 370 million in 2030 with the prevalence of the disease for all age groups to be 4.4%. 90% of diabetes cases worldwide are of Type II diabetes mellitus (T2DM) as a result of greater prevalence of sedentary lifestyle, unhealthy diet and rise of obesity, as well as an increasing number of elderly population. T2DM can be attributed to relative deficiency of insulin, involving insulin resistance, aberrant synthesis of hepatic glucose and progressive deterioration of pancreatic beta-cell functions resulting in chronic hyperglycaemia with disturbances in carbohydrate, fat and protein metabolism. Insulin resistance, classically defined as a decreased sensitivity to metabolic actions of insulin, is recognised as an important risk factor in the pathogenesis of various disorders, including T2DM. However, insulin resistance and ß-cell dysfunction can be asymptomatic and may remain undiagnosed for many years. Current T2DM management employs a range of pharmacological (hypoglycaemic agents) and lifestyle (diet, exercise) intervention approaches aiming at managing hyperglycaemia, with the main objective being to ensure sufficient delivery of glucose to the various tissues of the body and prevent hyperglycaemia by achieving good glycemic control. Nutrition has been regarded to play a significant role in the complex pathophysiology of T2DM and in the last several years, increasing amount of evidence has emerged linking various nutrients and food sources with a positive management of T2DM.

Seaweed have traditionally been consumed as a readily available whole food or traditional medical preparations, especially in Asia. Seaweeds are rich in bioactive compounds in the form of polyphenols, carotenoids, vitamins, minerals, phycobilins, phycocyanins, and polysaccharides, many of which are known to offer a wide range of benefits in human health.

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Pilot Exploratory Investigation Into the Effects of Brown Seaweed Extract Supplementation on Metabolic Biomarkers
Actual Study Start Date :
Jun 28, 2018
Actual Primary Completion Date :
Jan 30, 2020
Actual Study Completion Date :
Jan 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Placebo

3 capsules per day (1 before each meal) of cellulose

Dietary Supplement: Placebo
1 capsule 3 times per day

Active Comparator: Seaweed extract

3 capsules per day (1 before each meal) of seaweed extract

Dietary Supplement: Seaweed extract
1 capsule 3 times per day

Outcome Measures

Primary Outcome Measures

  1. Change in Plasma Glucose concentration [3 weeks]

    Changes in plasma glucose in healthy volunteers with BMI>25 after 3 weeks of treatment

  2. Change of Plasma Insulin concentration [3 weeks]

    Changes in plasma insulin in healthy volunteers with BMI>25 after 3 weeks of treatment

  3. Change in metabolic parameters [3 weeks]

    Changes in insulin sensitivity based on Homeostasis Model Assessment- Insulin Resistance (HOMA-IR) test

Secondary Outcome Measures

  1. Change in Blood Lipids [3 weeks]

    Changes in total cholesterol, HDL-C and triglycerides following 3 weeks supplementation

  2. Change in plasma Markers of inflammation [3 weeks]

    Changes in Tumor Necrosis Factor-alpha, Interleukin-6, Interleukin-1b, Interleukin-10, Interferon-gamma and C-Reactive Protein following 3 weeks of supplementation

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Body Mass Index (BMI) 25-35 kg/m2

  • Not dieting within the last month and not having lost >5% body weight in the previous year

  • Not increased physical activity levels in the past 2-4 weeks or intending to modify them during the study

  • Understands and is willing, able and likely to comply with all study procedures and restriction including being willing to follow the nutritional advice

  • Able to eat most everyday foods

  • Habitually consumes three standard meals a day

Exclusion Criteria:
  • Significant health problems (e.g. hypercholesterolaemia, diabetes, GI disorders)

  • Taking any medication or supplements known to affect mineral or glucose metabolism within the past month and/or during the study

  • Pregnant, planning to become pregnant or breastfeeding

  • History of anaphylaxis to food

  • Known allergies or intolerance to foods and/or to the study materials (or closely related compounds) or any of their stated ingredients

  • BMI <25 kg/m2 or >35 kg/m2

  • Volunteers self-reporting currently dieting or having lost >5% body weight in the previous year

  • Participants with abnormal eating behaviour

  • Participation in another experimental study or receipt of an investigational drug/product within 30 days of the screening visit

  • Volunteers who have significantly changed their physical activity in the past 2-4 weeks or who intend to change them during the study

  • Participants receiving systemic or local treatment likely to interfere with the evaluation of the study parameters

  • Participants on specific food avoidance diets

  • Participants who work in appetite or feeding related areas

Contacts and Locations

Locations

Site City State Country Postal Code
1 Roehampton University London United Kingdom SW15 5PJ

Sponsors and Collaborators

  • BioAtlantis Ltd.
  • University of Roehampton

Investigators

  • Study Director: George Tzortzis, BioAtlantis Ltd.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. George Tzortzis, Principle Investigator Human Health, BioAtlantis Ltd.
ClinicalTrials.gov Identifier:
NCT03853343
Other Study ID Numbers:
  • BioAtlDG001
First Posted:
Feb 25, 2019
Last Update Posted:
Mar 2, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 2, 2022