An interventional study of Healthy Nordic Diet and Usual Care in Coronary Disease, Coronary Arteriosclerosis and Myocardial Infarction, sponsored by Uppsala University. Recruiting at 1 site in Sweden. Open to participants aged 50 Years to 80 Years. Per ClinicalTrials.gov, last updated 2025-03-06.
Sponsored by Uppsala University · Not applicable, Interventional, and Treatment
Among 91 studies in Coronary Artery Disease with a site in Sweden — 13 open to participants now, 23 under way, 2 of them phase 3. Coronary Artery Disease · Sweden.
Among the 91 studies in Coronary Artery Disease with a site in Sweden, this one is the 49th largest by planned enrollment of the 70 interventional ones that give a count, is the only one that started in 2025, is one of 39 with no phase, reaches primary completion later than 20 of the 22 other live ones, and was the 89th registered.
4,857 studies on the registry are indexed under Coronary Artery Disease; 890 are open to participants now.
Browse Coronary Artery Disease studies →13 of the 91 studies in Coronary Artery Disease with a site in Sweden are open now. Recruiting first, the newest first:
Region Skane · Sites in Sweden
Ages 40+ · Healthy volunteers
CSL Behring · Sites in Sweden, United States, Argentina and 32 more countries
Ages 18+
Region Östergötland · Sites in Sweden
Ages 18+
Weill Medical College of Cornell University · Sites in Sweden, United States, Australia and 23 more countries
Ages 18+ · Women only
Vastra Gotaland Region · Sites in Sweden
Ages 18+
A study can be open while its sites in Sweden have not opened yet or have stopped. Only those recruiting at a site in Sweden →
Of the 588 Coronary Artery Disease studies recruiting now, 402 (68%) set no upper age limit and 68 (12%) stop at 75 or younger; 38 take children under 18; 47 take healthy volunteers.
This study: 50 Years to 80 Years · all sexes · no healthy volunteers.
The full table on the hub →This tab as a report to print or save as PDF → With an account.
91 studies; the count open now beside each. This study's row is marked.
A study in two phases is counted once above. Listed by phase, each with its combined phases: Phase 1 4 · Phase 2 12 · Phase 3 12 · Phase 4 5
First in 1992; this study’s year is marked. 1 started in 2025.
By drug class, each counting the studies that test any of its medicines:
This study's planned enrollment of 150 is above the median of 124 across 3,006 interventional studies indexed under Coronary Artery Disease.
Median enrollment 485 across the 70 interventional studies, 1,356 across the 21 observational. Of the 62 that completed or were terminated, 22 (35%) have results posted.
This tab as a report to print or save as PDF → With an account.
45 of 91 have an industry lead sponsor. The 10 most frequent:
Uppsala University is the lead sponsor of 390 studies on the registry; 86 are open to participants now.
Uppsala University has 2 studies filed under Coronary Artery Disease — fewer than ten, so there is no comparison to draw.
2 of the studies in Coronary Artery Disease with a site in Sweden that are under way reach primary completion within a year, 0 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT06578234Region SkaneHyperemic mYocardial Perfusion by adEnosine at diffeRent Doses | 2026-12-31 |
| NCT07884136Ribocure Pharmaceuticals ABRBD1119 in Coronary Artery Disease (CAD) | 2027-09-30 |
Among the 91 studies in Coronary Artery Disease with a site in Sweden, from their registry updates:
This tab as a report to print or save as PDF → With an account.
Diet can play a key role in atherosclerosis and coronary heart disease (CHD), but little interventional data exists, and the mediators of possible anti-atherosclerotic effects of diet are unclear. The investigators will investigate if a healthy Nordic diet (HND) reduces plaque volume, coronary artery calcification (CAC), and plaque inflammation (FAI) in CHD, and examine if changes in gut microbiota may be linked to plaque progression over time. The investigators will also explore if the diet response can be predicted by the metabolic phenotype.
In total 150 CHD patients is randomized to a HND rich in unsaturated fat and fibre from plants, or to a "usual care diet" for 18 months. Plaque volume and composition is assessed by CT, and fecal microbiota composition is determined by deep metagenome shotgun sequencing. CHD and metabolic risk factors, liver fat, muscle fat and biomarkers of diet adherence (plasma fatty acids, whole-grain metabolites) are measured. Machine-learning is used to identify diet "responders" on plaque progression, based on the individual microbiome and metabolome.
If a HND reduces plaque progression, this would be novel information of clinical importance. Also, if the diet alters microbiota that are linked to plaque progression, this would be of high scientific interest. Finally, potential prediction of the diet-response would open up for more personalized treatment of atherosclerosis.
Atherosclerosis of coronary arteries is the main cause of coronary heart disease (CHD). In atherosclerosis, atherogenic lipids are deposited in the arteries to form plaques, and the larger the plaque volume, the more narrowing of the vessel. It is now feasible to directly visualize clinically relevant changes in plaque volume and composition (e.g. calcification, lipid content) by modern computed tomography (CT) angiography. Diet is a cornerstone in both primary and secondary prevention, but it is still not clear if dietary intervention can reduce coronary plaque progression as assessed by modern imaging technique.
In the Nordic countries, a promising alternative to Mediterranean diets is the Healthy Nordic diet. Controlled trials conducted in various Nordic populations have shown that healthy Nordic diets cause reduction of several key CVD risk factors such as elevated blood lipids and blood pressure, hyperglycemia, and inflammation. The Healthy Nordic diet is mainly, but not exclusively, a plant-based diet that accord with the Nordic Nutrition Recommendations (NNR 2023), e.g. is rich in vegetable fats from oils, spreads, nuts and seeds, whole-grains from rye, barley and oats, legumes, vegetables, Nordic fruits and berries but with moderate portions (2-3 times per week) of fatty fish (e.g. Salmon). The effects of a Healthy Nordic diet in a secondary preventive setting and in particular the potential impact on atherosclerosis is yet unknown. The investigators hypothesize that a Healthy Nordic Diet has anti-atherosclerotic properties that can reduce the progress of atherosclerosis and reduce key CVD risk markers and inflammation in patients with a recent MI or chronic coronary syndrome (CCS). Further, the investigators hypothesize this diet will have favorable changes on the gut microbiota, which in turn can contribute to reduced coronary plaque progression.
The overall aim is to compare the ability of a Healthy Nordic Diet versus usual care dietary advice to influence coronary plaque volume and CVD risk after 18 months in patients with MI or with CCS.
The primary aim is to investigate if a Healthy Nordic Diet can reduce plaque volume after 18 months as compared with usual care and routine dietary and lifestyle advice, and secondary aims are to investigate dietary effects on plaque composition, coronary artery calcium (CAC) and coronary inflammation (perivascular fat, fat attenuation index), as well as on ectopic fat content (e.g. liver). Exploratory aims are to investigate the dietary effects on gut microbiota, as well as on metabolomic- lipidomic- and proteomic plasma profiles. In addition, the investigators will monitor blood glucose control using wearable continous glucose monitors (CGMs) as well as Actiheart monitors to record heart ECG and activity with multiple data endpoints.
This study, named NORDHEART, is a randomized, single-blinded, parallel study including a dietary intervention group and a control group, in individuals with diagnosed MI or CCS. The investigators aim to include n=150 individuals in this trial. The majority of participants will be recruited at the Uppsala University hospital but further Swedish recruitment center in mid Sweden might be added if the recruitment rate in Uppsala is slower than expected.
Inclusion criteria include men and women with diagnosed MI from 2 weeks after diagnosis and 6 months after diagnosis, or with CCS (e.g. stable angina pectoris), ages 50 to 80 years, BMI 25-40.
The intervention diet consists of advice to follow a Healthy Nordic Diet as, and it will be advised ad libitum. Certain key food items will be provided (\~5 E%) to participants in the intervention. The control group ("usual care") will receive dietary advice in accordance with routine clinical procedures at the cardiology clinic at the Uppsala academic hospital, which follows the national guidelines for lifestyle advice in CVD care.
To monitor dietary intake in both groups, 4-day food records will be conducted at baseline, 6 months, 12 months and 18 months after study entry. Plasma fatty acid composition will be measured to objectively monitor any changes in dietary fat quality, and serum alkylresorcinols will be assessed as valid biomarkers of whole-grain intake from rye and wheat.
The primary outcome is difference between the groups in change in coronary artery plaque volume from baseline to 18 months. Intention-to treat analyses will be the primary analyses.
Secondary outcomes are change in plaque composition and inflammation (perivascular fat and inflammation, coronary calcification [CAC score], liver fat and hepatic fibrosis, LDL-cholesterol, HDL-cholesterol, ApoB, triglycerides, HbA1c, inflammation markers, from baseline to 18months, and a composite of atherosclerotic cardiovascular disease events during the 18 month follow-up.
Exploratory outcomes include effects on gut microbiota, and proteins and lipids (e.g. ceramides) involved in inflammation and markers of the atherosclerotic process. In addition, prediction models using lipidomics, metabolomics, proteomics and genetics will be assessed to explore determinants of responders and non-responders to the dietary intervention, with regard to effects on plaque volume and composition.
The plaque volume and plaque composition with be assessed by novel photon-counting CT angiography (CCTA). This technique can identify and characterize subclinical atherosclerotic disease in most vascular beds, and will be assessed at baseline and 18 months.
Given the large patient group of CHD worldwide, the clinical significance of this study has large potential, especially since there is still only limited evidence to suggest that intense dietary intervention might halt the atherosclerotic progress per se.
4,857 studies on the registry are indexed under Coronary Artery Disease; 890 are open to participants now.
This study's planned enrollment of 150 is above the median of 124 across 3,006 interventional studies indexed under Coronary Artery Disease.
Browse Coronary Artery Disease studies →Uppsala University is the lead sponsor of 390 studies on the registry; 86 are open to participants now.
Compared within Coronary Artery Disease, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Coronary Disease. The counts are of registry records indexed under each term, refreshed daily. How we classify →
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.
What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.
The New York Heart Association’s four classes of how much heart failure limits physical activity.
Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
BMI (body mass index)
Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.
What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
NYHA class (heart failure)
The New York Heart Association’s four classes of how much heart failure limits physical activity.
Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Life expectancy
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Dietary advice and provided with some key food items of the healthy Nordic diet
Other: Healthy Nordic Diet
Dietary advice according to standard clinical care at the cardiology unit
Behavioral: Usual Care
Participants will be adviced a healthy Nordic diet and will also receive certain Nordic foods high in wholegrains and polyunsaturated fat from vegetable sources
Usual care lifestyle advice and national and general recommendations on diet
Change in coronary plaque volume
Will be assessed by photon-counting CT angiography
Time frame: 18 months
Change in coronary inflammation: Fat attenuation Index
Perivascular fat will be assessed by photon counting CT angiography
Time frame: 18 months
To investigate if a Healthy Nordic Diet can decrease progression of atherosclerosis Change in coronary artery calcium score (CACS)
CACS will be assessed by photon counting CT angiography
Time frame: 18 months
Change in ectopic fat (liver, heart, muscle)
Will be assessed by photon counting CT angiography
Time frame: 18 months
Change in blood glycemic control
Will be measured in fasting state and continously using CGM
Time frame: 6, 12 and 18 months
Change in plasma LDL cholesterol
Will be assessed by routine methods at the hospital lab
Time frame: 18 months
Change in systolic and diastolic blood pressure
Time frame: 6, 12 and 18 months
Incident cardiovascular events
A composite outcome will be assesed
Time frame: 18 and 30 months (12 month post intervention)
Change in hepatic fibrosis
Liver stifness and fibrosis stages assessed by Fibroscan
Time frame: 18 months
Change in gut microbiota
Gut microbiota will be measured in fecal samples
Time frame: 12 and 18 months
Change in plasma inflammation proteins
Protemomic approcah will be used
Time frame: 6, 12 and 18 months
Change in plasma lipidomic profile including ceramides
Lipidomic approach will be used
Time frame: 6, 12 and 18 months
Change in plasma metabolite pattern
A metabolomic approach will be used
Time frame: 6, 12 and 18months
Plan to share: Undecided
No publications or documents are linked to this record.
Start is estimated for Mar 2025; primary completion for Jun 2030, 63 months later.
Of 753 non-industry interventional studies with no phase under Coronary Artery Disease, half reached primary completion within 33 months of starting (the median), counting those still running; a quarter within 15 and three quarters within 53. This study's planned 63 months is above that.
Counting every sponsor, half of 930 studies reached it within 30 months; a quarter within 15 and three quarters within 50.
How these figures are worked out, and which studies are left out of them.
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