NCT03620266Active, not recruiting
Effects of Bilberry and Oat Intake After Type 2 Diabetes and/or MI
Effects of Bilberry and Oat Intake on Plasma Lipid Profile, Inflammation, and Exercise Capacity in Patients With Type 2 Diabetes and/or Myocardial Infarction (BioDiaMI): a Randomized, Double-blind, Placebo-controlled Trial
Source: ClinicalTrials.gov · Last updated 23 Mar 2026
Brief summary (registry, in English)
Background: Bilberries from Sweden, rich in polyphenols, have shown cholesterol-lowering effects in small studies, and the cholesterol-lowering properties of oats, with abundant beta-glucans and potentially bioactive phytochemicals, are well established. Both may provide cardiometabolic benefits for patients with manifest chronic cardiometabolic disease, such as type 2 diabets mellitus (T2DM) and myocardial infarction (MI). However, large studies of adequate statistical power and appropriate duration are needed to confirm clinically relevant treatment effects. No previous study has evaluated the potential additive or synergistic effects of bilberry combined with oats on cardiometabolic risk factors. Design: This is a double-blind, randomized, placebo-controlled clinical trial. Our primary objective is to assess cardioprotective effects of diet supplementation with dried bilberry and with bioprocessed oat bran, with a secondary explorative objective of assessing their combination, compared with a neutral isocaloric reference supplement, for patients diagnosed with T2DM and/or MI. Patients will be randomized 1:1:1:1 to a three-month intervention. The primary endpoint is the difference in LDL cholesterol change between the intervention groups after three months. The major secondary endpoint is exercise capacity at three months. Other secondary endpoints include plasma concentrations of biochemical markers of inflammation, glycaemia, and gut microbiota composition after three months. Implications: Secondary prevention after cardiometabolic disease, including T2DM and MI, has improved during the last decades but diabetes complications, readmissions and cadiovascular related deaths following these conditions remain large health care challenges. Controlling hyperlipidemia, hyperglycaemia, hypertension and inflammation is critical to preventing (new) cardiovascular events, but novel pharmacological treatments for these conditions are expensive and associated with negative side effects. If bilberry and/or oat, in addition to standard medical therapy, can lower LDL cholesterol and inflammation more than standard therapy alone, this could be a cost-effective and safe dietary strategy for secondary prevention in high-risk patients or risk prevention in subjects with T2DM.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 900 (estimated)
- First submitted
- 2 Aug 2018
- Start date
- 30 Sept 2021
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- Ole Frobert, MD, PhD
- Diseases
- Coronary artery disease, Type 2 diabetes
- NCT number
- NCT03620266
What you commit to
- Study type: Interventional
- Planned participants: 900
- From 30 Sept 2021 to the primary completion date, 31 Dec 2026
- 8 sites in 2 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous randomization in the BioDiaMI trial
Other illness
- Food allergy/intolerance to gluten, bilberries or legumes
Lab values
- LDL cholesterol \<2.0 mmol/L
Age
- \<18 years of age
Other
- Emergency coronary artery bypass grafting
- Daily intake or the intent to initiate daily intake of bilberry in any form or daily intake of \>15 g of oatmeal or equivalent
- Inability to provide informed consent
Who the study is looking for
- Confirmed T2DM diagnosis (any treatment modality accepted) and/or within 3 years post STEMI or NSTEMI
- Completed coronary angiography/PCI
- Male and female subjects ≥18 years
- Allocated to atorvastatin at a daily dose of 80 mg (only eligible for patients enrolled up to 7 days post MI and not for T2D subjects)
- Written informed consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (8)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Steno Diabetes center Coordinator of this site? Confirm its status | Aarhus | Denmark | Unknown status |
| Odense University Hospital Coordinator of this site? Confirm its status | Odense | Denmark | Unknown status |
| Falu Lasarett Coordinator of this site? Confirm its status | Falun | Sweden | Unknown status |
| Sahlgrenska Universitetssjukhuset Coordinator of this site? Confirm its status | Gothenburg | Sweden | Unknown status |
| Karlstad general hospital Coordinator of this site? Confirm its status | Karlstad | Sweden | Unknown status |
| Department of Cardiology, Skånes universitetssjukhus Coordinator of this site? Confirm its status | Lund | Sweden | Unknown status |
| Department of Cardiology, Örebro University Hospital Coordinator of this site? Confirm its status | Örebro | Sweden | Unknown status |
| Cardiology Clinic, Västmanlands sjukhus Coordinator of this site? Confirm its status | Västerås | Sweden | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.