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NCT07366710Active, not recruiting

Measuring Amino Acid and Glucose Metabolism in Healthy Volunteers and NAFLD Patients Using Total-body PET

Quantification of Amino Acid and Glucose Metabolism in Healthy Controls and Patients With Non-alcoholic Fatty Liver Disease Using Total- Body PET

Source: ClinicalTrials.gov · Last updated 2 Feb 2026

Brief summary (registry, in English)

This observational study aims to quantify whole-body amino acid and glucose metabolism in healthy adults and in patients with non-alcoholic fatty liver disease (NAFLD) using total-body PET/CT. The study investigates how orally and intravenously administered PET tracers (18F-FDG and 18F-FET) are absorbed in the gastrointestinal tract, distributed across major organs, and metabolized in different physiological and pathological states. A further objective is to examine how glucagon, during a pancreatic clamp using somatostatin, influences amino acid metabolism in healthy individuals and whether this response is altered in patients with NAFLD. Participants will be healthy volunteers or patients with NAFLD, aged 18-70 years. Depending on study group, participants will undergo one or more total-body PET/CT scans following oral or intravenous tracer administration, and in some cases receive glucagon or placebo infusion. Blood samples will be collected during scanning to assess hormone levels and metabolic responses. Data from these imaging sessions will be used to characterize nutrient metabolism, compare oral and intravenous tracer kinetics, and explore glucagon-induced metabolic changes across study groups.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
36 (estimated)
First submitted
16 Jan 2026
Start date
5 Nov 2024
Primary completion date
Oct 2027
Lead sponsor
Copenhagen University Hospital, Rigshospitalet
NCT number
NCT07366710

What you commit to

  • Study type: Interventional
  • Planned participants: 36
  • From 5 Nov 2024 to the primary completion date, Oct 2027
  • 1 site in 1 country
  • 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.

Other illness

  • Diabetes, cancer (active or treated within the last five years) or inflammatory diseases.
  • Chronic disorders that require medical treatment

Lab values

  • Low albumin

Other

  • Pregnancy
  • Claustrophobia
  • Inability to give consent due to psychological or other causes
  • Inability to speak/read Danish

Who the study is looking for

  • Age 18-70 years
  • Body mass index (BMI) 20-27 kg/m2

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Copenhagen University Hospital, Rigshospitalet
Coordinator of this site? Confirm its status
CopenhagenDenmarkUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.