We hypothesize that dietary supplementation with seaweed will improve glucose regulation in T2DM patients.
ID
Source
Brief title
Health condition
diabetes type 2
Sponsors and support
Intervention
Outcome measures
Primary outcome
Difference between the mean blood glucose levels measured during the first week of usual diet and during week 2 to 6 when daily seaweed is consumed.
Secondary outcome
differences between week 1 and week 6 in terms of body weight (kg); HbA1c and total daily insulin use, and fasting blood glucose levels (Mmol/L) in addition to the continuously monitored glucose levels. Levels of total cholesterol, LDL-cholesterol, HDL-cholesterol, lipoprotein (a) (g/L), apoB100/48 (Mmol/L) and triglycerides (Mmol/L) (measured using routine laboratory analysis) will be analyzed, and pulse wave velocity and blood pressure (mmHg) and cytokines.
Background summary
Rationale: Type 2 diabetes mellitus (T2DM) is a serious highly prevalent (> 1 million in the Netherlands) chronic disease and its complications, cardiovascular disease, retinopathy, nephropathy, neuropathy, and foot amputation lead to premature death. Therefore there is an urge for prevention. Because diet plays an important role in the development of T2DM, dietary interventions may provide solutions. Seaweeds contain unique bioactive components that improve glucose tolerance and also circulating lipid levels. Objective: To determine if dietary supplementation with seaweed improves glucose regulation in T2DM patients. Study design: This is a randomized placebo-controlled study to be conducted in three parallel study arms for 6 weeks. Study population: Sixty eligible patients with T2DM and a BMI > 25 will be enrolled. The study will be performed in patients with T2D and a BMI>25 The participants are allowed for inclusion in the study only after written informed consent and approval by our Medical Ethical Review Board. Exclusion criteria are type 1 or monogenetic forms of diabetes, thyroid disease, pregnancy use of blood coagulants and corticosteroids, heart failure and recent myocardial infarction The participants are allowed for inclusion in the study only after written informed consent and approval by our Medical Ethical Review Board. Intervention (if applicable): Patients will receive either 5 gram of Sargassum fusiforme (Sargassum), Fucus vesiculosus (Fucus) or placebo (0.5 gram Nori) during 5 weeks (week 2-6). Clinical information (anamnesis and physiological examination) and blood sampling will be performed at the start of the study, 1 week and after 6 weeks of the study. One week before start of the treatment and during treatment blood glucose will be monitored continuously by a device, that will be replaced weekly, blinded for the participants. This study will be conducted in compliance with Good Clinical Practices (GCP) and ICH guidelines Main study parameters/endpoints: Main study parameters/endpoints: Difference between the mean blood glucose levels measured during the first week of usual diet and during week 2 to 6 when daily seaweed is consumed. Secondary outcomes are differences between week 1 and week 6 in terms of body weight (kg) because seaweed consumption can contribute to weight loss; HbA1c and total daily insulin use, and fasting blood glucose levels (Mmol/L) in addition to the continuously monitored glucose levels. Levels of total cholesterol, LDL-cholesterol, HDL-cholesterol, lipoprotein (a) (g/L), apoB100/48 (Mmol/L) and triglycerides (Mmol/L) (measured using routine laboratory analysis) will be analyzed, and pulse wave velocity and blood pressure (mmHg) and cytokines.
Study objective
We hypothesize that dietary supplementation with seaweed will improve glucose regulation in T2DM patients.
Study design
baseline (week 1) - week 2-6 (continuous glucose monitoring)
Intervention
Patients will receive either 5 gram of Sargassum fusiforme (Sargassum), 5 gram of Fucus vesiculosus (Fucus) or placebo (0.5 gram Nori) during 5 weeks (week 2-6).
Inclusion criteria
- Patients with T2DM and BMI>25 - All adults; age ≥ 18 years - Diabetes based on criteria of ADA
Exclusion criteria
- Type 1 or monogenetic forms of diabetes. - Thyroid disease - Pregnancy - Usage of corticosteroids - Usage of blood anti-coagulants - History of heart failure or recent myocardial infarction within 3 months - Transplantation - Allergy for shellfish
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL7987 |
CCMO | NL66189.078.18 |