Taking people in DenmarkPhase 2
Imaging brain tumors with hyperpolarized pyruvate MRI
Tests a special pyruvate MRI scan in adults with glioblastoma brain tumors.
Key facts
- Who runs it
- Aarhus Universitet
- Where
- Aarhus N, DenmarkSee the site
- Registry title
- MRI with hyperpolarized pyruvate in gliblastoma - a phase II study
- Status
- Recruiting
- Phase
- Phase 2
- People taking part
- 10 people, planned
- Started
- 1 Apr 2020
- Expected to end
- 31 Dec 2027
- Type of study
- Interventional
- Record updated
- 28 November 2025
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 newly diagnosed high-grade glioma (grade 3 or 4) who are about to start radiotherapy.
- Age
- At least 18 years old.
- Sex
- All sexes can join.
- Disease stage
- Newly diagnosed high-grade glioma (grade 3 and 4), scheduled for radiotherapy. WHO performance status 0-2.
- Earlier treatment
- No previous or current radiation or chemotherapy. No other investigational agents.
Main reasons for not taking part
- Allergy to pyruvate
- Cannot have an MRI (for example pacemaker, metal in the body, claustrophobia)
- Cannot have gadolinium contrast (eGFR 30 mL/min/1.73m2 or less, or earlier reactions to it)
- Expected remaining survival under 3 months
- Symptomatic heart disease, or history of alcohol abuse or illicit drug use
The registry criteria, word for word
Show all 16 criteriaShow less
Who can take part
- Patients with newly diagnosed high-grade glioma (grade 3 and 4)
- Scheduled for radiotherapy
- At least 18 years of age
- WHO performance status 0-2
- Women who are not postmenopausal or surgically sterile must have a negative serum or urine pregnancy test performed at time of inclusion in the study. Safe and highly effective contraception must be used throughout the study meaning either hormonal anti-conception or an anti-fertility intrauterine device. If the partner is non fertile or the patient has no sexual activities, this is also accepted
- Danish speaking
- Able and willing to comply after informed consent
Who cannot take part
- Not able or willing to receive radiotherapy
- Subjects who are receiving any other investigational agents
- Previous or current treatment by radiation or chemotherapy
- History of alcohol abuse or illicit drug use
- Allergy to pyruvate
- Contraindications to MRI o Pacemaker, neurostimulator or cochlea implant o Metal foreign bodies such as fragments and irremovable piercings o Unsafe medical implants (safety of heart valves, hips and the like must be confirmed) o Intracranial clips or coils o Claustrophobia o Largest circumference including arms > 160 cm
- Symptomatic cardiac disease (i.e. valve disease, coronary artery disease, arrythmias etc.). Hypertension and hyperlipidemia are allowed
- Contraindications to gadolinium contrast o eGFR ≤ 30 mL/min/1.73m2 o Previous adverse reactions to gadolinium
- Predicted remaining survival <3 months
Where in Denmark
- Aarhus UniversitetAarhus N, DenmarkTaking people
About the trial
What the trial wants to find out
We hypothesis that tumor and therapy related changes in the brain tissue are associated with altered metabolic profiles and this is detectable with hyperpolarized [1-13C]pyruvate MRI.
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record
Print a page for my doctorData and sources
- Registry record
- Listed on the EU's official list of trials (CTIS).
- Official title
- MRI with hyperpolarized pyruvate in gliblastoma - a phase II study
- Plain-language title
- Imaging brain tumors with hyperpolarized pyruvate MRIGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 9 November 2026.
- Record updated
- 28 November 2025