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2024-512490-27-00RecruitingPhase 2

Early detection of hepatocellular carcinoma by Hyperpolarized [1- 13C]pyruvate MRI

Source: EU CTIS (euclinicaltrials.eu) · Last updated 29 Aug 2026

Next steps

Brief summary (registry, in English)

This project seeks to determine the potential of hyperpolarized pyruvate MRI in early characterization of primary liver cancer - particularly small tumors.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
46 (estimated)
First submitted
8 Jul 2024
Start date
19 Jun 2023
Lead sponsor
Aarhus Universitet
EU CT number
2024-512490-27-00
EudraCT number
2021-000863-56

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 46
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Pacemaker, neurostimulator or cholera implant

Other illness

  • Chronic kidney disease
  • Competing systemic disease (hypertension, dyslipidemia, diabetes etc. allowed)
  • Allergy to pyruvate
  • Significant cardiac disease (as left ventricular outflow obstruction or heart failure)
  • Significant obstructive lung disease or severe asthma
  • Unsafe medical implants (safety of heart valves, hips and the like must be confirmed)

Lab values

  • Patients with tumors must have eGFR > 30 ml/min/1.73m2

Other

  • Contraindications for MRI with contrast:
  • Hepatic encephalopathy ≥ grade 2.
  • Stents or other devices implanted close to the liver that may cause imaging artefacts
  • Metal foreign bodies such as fragments and irremovable piercings
  • Largest circumference including arms > 160 cm
  • Claustrophobia

Who the study is looking for

  • Aged 18 – 85 years. The age and gender of the healthy controls of the main study will be matched to the participating patients.
  • Pre-menopausal women must be confirmed non-pregnant by an onsite test
  • HCC group: - Diagnosed HCC larger than 10 mm confirmed by standard MRI, CT or confirmed by tumour biopsy. - Subgroup 1: Not elected for liver surgery - Subgroup 2: Elected for liver surgery
  • Small tumor group: - One or more small lesions in the liver requiring 2 years of repeated follow-up as per the EASL guideline. Could be in a liver with a confirmed HCC.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Aarhus UniversitetshospitalAarhus NDenmarkRecruiting

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