ClinicalTrials.gg
RecruitingNCT06701968NORDHEARTUpdated Mar 6, 2025

Effects of a Healthy Nordic Diet on Atherosclerosis in Patients with Coronary Heart Disease

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.

Primary conditionCoronary Artery DiseaseRegistry: Coronary DiseaseReclassifiedWhy we changed it
Registry
Coronary Disease — the first condition term the registry derived for this study.
ClinicalTrials.gg
Coronary Artery Disease
Why
  1. The study's listed conditions name Coronary Artery Disease, a narrower term within Coronary Disease.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Uppsala University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
150
Allocation
Randomized
Ages
50 Years to 80 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

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.

Planned enrollment
49th of 70
150 · median 485
Started
2025
the only one that year
No phase
39 of 91
7 open now
Primary completion
2030-06
later than 20 of 22 live
Registered
89th of 91
by date

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.

Coronary Artery Disease

4,857 studies on the registry are indexed under Coronary Artery Disease; 890 are open to participants now.

Browse Coronary Artery Disease studies →

Open to participants now

13 of the 91 studies in Coronary Artery Disease with a site in Sweden are open now. Recruiting first, the newest first:

7 more — sign in →

All 13 open studies →

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 →

Who these studies take

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.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 91 studies in Coronary Artery Disease with a site in Sweden, or all of them as a file.
02

Study summary

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.

Read the detailed description

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.

03

Conditions studied

  • Coronary Disease
  • Coronary Arteriosclerosis
  • Myocardial Infarction
  • Chronic Coronary Syndrome
  • MASLD
  • Type 2 Diabetes

Keywords

  • Diet
  • Secondary prevention
  • Coronary plaque regression
  • Atherosclerosis
  • Type 2 diabetes
  • Coronary heart disease
  • Myocardial infarction
  • Coronary computed tomography angiography
  • Healthy nordic diet
  • NAFLD
04

In context

Coronary Artery Disease Reclassified

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 →

Lead sponsor

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 →

05

Who can participate

Ages eligible
50 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

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.

Inclusion criteria

  • Men and women
  • Diagnosis with MI from 2 weeks after diagnosis and with maximum 6 months after diagnosis
  • Diagnosis with CCS (e.g. stable angina pectoris)
  • Ages 50 to 80 years
  • 25-40.

Exclusion criteria

Exclusion Criteria:

  • Severe heart failure ( classes III, IV)
  • Alcohol intake >20g/day
  • Unwillingness to follow a new prescribed diet for 18 months
  • Other diseases implying a short estimated (e.g. severe malignant or kidney or liver disease, as judged by consenting physician).
Terms in these criteria, in plain language(3)

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.

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.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

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.

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.

06

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
150 participants (estimated)

Study arms

  • Experimental
    Healthy Nordic Diet

    Dietary advice and provided with some key food items of the healthy Nordic diet

    Other: Healthy Nordic Diet

  • Active comparator
    Usual care

    Dietary advice according to standard clinical care at the cardiology unit

    Behavioral: Usual Care

Interventions

  • OtherHealthy Nordic Diet

    Participants will be adviced a healthy Nordic diet and will also receive certain Nordic foods high in wholegrains and polyunsaturated fat from vegetable sources

  • BehavioralUsual Care

    Usual care lifestyle advice and national and general recommendations on diet

07

What researchers measure

Primary outcomes

  1. Change in coronary plaque volume

    Will be assessed by photon-counting CT angiography

    Time frame: 18 months

Secondary outcomes

  1. Change in coronary inflammation: Fat attenuation Index

    Perivascular fat will be assessed by photon counting CT angiography

    Time frame: 18 months

  2. 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

  3. Change in ectopic fat (liver, heart, muscle)

    Will be assessed by photon counting CT angiography

    Time frame: 18 months

  4. Change in blood glycemic control

    Will be measured in fasting state and continously using CGM

    Time frame: 6, 12 and 18 months

  5. Change in plasma LDL cholesterol

    Will be assessed by routine methods at the hospital lab

    Time frame: 18 months

  6. Change in systolic and diastolic blood pressure

    Time frame: 6, 12 and 18 months

  7. Incident cardiovascular events

    A composite outcome will be assesed

    Time frame: 18 and 30 months (12 month post intervention)

  8. Change in hepatic fibrosis

    Liver stifness and fibrosis stages assessed by Fibroscan

    Time frame: 18 months

Other outcomes

  1. Change in gut microbiota

    Gut microbiota will be measured in fecal samples

    Time frame: 12 and 18 months

  2. Change in plasma inflammation proteins

    Protemomic approcah will be used

    Time frame: 6, 12 and 18 months

  3. Change in plasma lipidomic profile including ceramides

    Lipidomic approach will be used

    Time frame: 6, 12 and 18 months

  4. Change in plasma metabolite pattern

    A metabolomic approach will be used

    Time frame: 6, 12 and 18months

08

Study locations

1 of 1 sites recruiting
  • Cardiology clinic, Uppsala university hospital
    Uppsala, Sweden
    Recruiting
09

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

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.

Registered
Nov 19, 2024
First posted
Nov 22, 2024
StartEst.
Mar 20, 2025
Primary completionEst.
Jun 30, 2030
CompletionEst.
Dec 30, 2031
Last update
Mar 6, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 6, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT06701968
Lead sponsor
Uppsala University
Collaborators
Falu Hospital
Responsible party
Ulf Risérus (Professor, Uppsala University) — Principal investigator
First posted
Nov 22, 2024
Start date
Mar 20, 2025 (estimated)
Primary completion
Jun 30, 2030 (estimated)
Completion
Dec 30, 2031 (estimated)
Last update
Mar 6, 2025

Study contacts

Emil Hagström, MD, PHD
Contact
emil.hagstrom@ucr.uu.se
46184710000
Fredrik Rosqvist, PHD
Contact
fredrik.rosqvist@uu.se
Ulf Risérus, MMED, PHD
principal investigator · Uppsala University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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