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Semaglutide and Fat Inside the Heart and Leg Muscles in Type 2 Diabetes

Tests semaglutide with diet and exercise advice in adults with type 2 diabetes.

Key facts

Who runs it
University of Aberdeen
Where
Aberdeen, United KingdomSee the site
Trial code
Registry title
Rebalancing the Fat Content of the Heart and Muscles
Status
Recruiting
People taking part
60 people, planned
Started
1 Aug 2025
Expected to end
31 Jul 2028
Type of study
Interventional, 2 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • Semaglutide administration plus dietary counselling and physical activity encouragement
  • Semaglutide plus a personalised and supervised program of resistance and endurance training
Record updated
30 April 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with type 2 diabetes diagnosed in the last 10 years, who are overweight, not very active and not on insulin.

Age
20 to 75 years
Sex
All sexes can join
Disease stage
Type 2 diabetes confirmed within the previous 10 years, with HbA1c of 53 mmol/mol (7%) or higher; BMI of 27 or higher with body weight under 140kgs; kidney function (eGFR) above 30 mL/min/1.73m2
Earlier treatment
Usually on diet and/or metformin/sulphonylureas (and/or sodium-glucose cotransporter-2 inhibitors, Dipeptidyl peptidase 4 inhibitors, thiazolidinediones), but not on insulin; not doing more than 150 minutes per week of moderate-vigorous physical activity

Main reasons for not taking part

  • Known heart disease or coronary artery disease
  • Taking other glucagon-like peptide-1 receptor agonists, niacin or omega-3 fatty acids
  • Sensitivity to Semaglutide, including pancreatitis, diabetic retinopathy or any cancer
  • Pregnancy, breastfeeding or considering pregnancy
  • Unable to cycle, exercise or fit in the magnetic resonance scanner

The registry criteria, word for word

Show all 25 criteriaShow less

Who can take part

  • Patients with a confirmed diagnosis of type 2 diabetes established in the previous 10 years between the ages of 20 and 75
  • HbA1c ≥ 53 mmol/mol (7%) typically on diet and/or metformin/sulphonylureas (and/or sodium-glucose cotransporter-2 inhibitors, Dipeptidyl peptidase 4 inhibitors, thiazolidinediones, but not on insulin)
  • Patients who do not meet the WHO recommendations on physical activity (≤150 minutes per week) of moderate-vigorous physical activity (MVPA)
  • Patients who have a BMI of ≥27 but with a body weight of less than 140kgs due to limitations of the scanner table weight limit
  • Current or recent (within 3 months) eGFR >30 mL/min/1.73m2)
  • Able to understand written and spoken English

Who cannot take part

  • Any previously unknown cardiac condition other than mild valvular disease
  • Patients with any dietary habits that may interfere with the investigation (for example high fat vegan diets, as we know form prior research that they have very different intramyocellular fat storage compared to those on no dietary preferences)
  • Any history of known coronary artery disease (including myocardial infarction and myocardial infarction with normal coronary arteries)
  • Any relevant or untreated endocrine condition (i.e. Cushings)
  • Patients with any history of any medical or surgical condition that in the judgement of the investigators may interfere with the exercise regime (i.e. peripheral vascular disease, arthritis), fatty acids metabolism (i.e. lipid storage diseases) or may compromise the safety of the participant (i.e. neurological syndromes for whom an intense exercise program could result in musculo-skeletal injury or accidents due to loss of balance)
  • Patients with a sensitivity to Semaglutide (known hypersensitivity, diabetic retinopathy, pregnancy, history of pancreatitis or history of any cancer)
  • Significant asthma or pulmonary disease
  • Patients on any other medication known to influence glucose or fatty acids metabolism (niacin, omega-3 fatty acids, other glucagon-like peptide-1 receptor agonists)
  • Impaired renal function (defined as estimated glomerular filtration rate of less than 30 mL/min/1.73m2)
  • Blood pressure of more than 180/100 mmHg
  • Participants unable to cycle on the ergometer
  • Unable to perform exercise testing (e.g. prosthetic limbs)
  • Pregnancy, breastfeeding or considering pregnancy
  • Patients who have recently had gastrointestinal contrast or radionuclides
  • Inability to lie flat or remain motionless for scanning procedures
  • Patients whose girth size cannot allow them to fit in the magnetic resonance scanner (there is no set location to measure as this is different for everyone, but we have a plastic hoop that can be fitted around the largest circumference to check the fit)
  • Subjects who are not able to engage into a physical training regime or feel that they do not have the interest or sustained motivation to follow one
  • Participants currently enrolled in other interventional clinical research
  • Participants not able to understand written or verbal English

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 20 and 75 years old?

Where in United Kingdom

  • Cardiac Research Office, Aberdeen Royal InfirmaryAberdeen, United KingdomContact: Dana Dawson, PhDTaking people

About the trial

What the trial wants to find out

Traditional diabetes therapies focus on improving blood sugar control. However, many studies show that this may not be enough. New treatments focusing on weight loss have heralded better results. One of these treatments is Semaglutide and the investigators wish to examine its effects further in this study. The investigators propose to investigate what happens to the fat inside the heart and the leg muscles.

The 2 groups in the trial

  • Semaglutide administration plus dietary counselling and physical activity encouragementPlacebo, for comparison
  • Semaglutide and supervised training programExisting treatment, for comparison

    Semaglutide administration plus a personalised and supervised program of resistance and endurance training

    Treatment: Semaglutide plus a personalised and supervised program of resistance and endurance training

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Intramyocellular Lipid Compartments After Glucagon-like Peptide 1 Receptor Agonist Therapy in Type 2 Diabetes - Rebalancing the Fat Content of the Heart and Muscles
Plain-language title
Semaglutide and Fat Inside the Heart and Leg Muscles in Type 2 DiabetesGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Fit questions
Built from NCT07065383, who can take part
Record updated
30 April 2026