Clinical trial Recruiting at 1 site Phase 1 Interventional Ages 18 to 80

Using advanced MRI to diagnose brain tumors

Official title: Correlation of Hyperpolarized 13C-pyruvate Metabolic Magnetic Resonance Imaging and Tumor Histopathology in Patients With Infiltrating Gliomas

Run by University of Maryland, Baltimore · NCT04772456 · Data updated 2026-11-12

This study is testing a new type of MRI to see if it can better identify brain tumors called infiltrating gliomas in patients who are about to have surgery.

Quick facts

PhasePhase 1
Study typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment5 (estimated)
SponsorUniversity of Maryland, Baltimore
Academic / other
Locations1 site (Baltimore, Maryland)
StatusRecruiting
StartedAugust 11, 2020
Main results expectedAugust 31, 2026
Study endsDecember 31, 2027
Registry record updatedSeptember 22, 2025
Trial IDNCT04772456 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18-80 with suspected infiltrating gliomas or a history of such tumors who can undergo MRI.

Probably not a fit

Patients unable to undergo MRI or those with severe reactions to IV contrast may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to evaluate the safety and feasibility of hyperpolarized metabolic MRI for diagnosing infiltrating gliomas, a type of brain tumor. It will assess how accurately this advanced imaging technique can identify these tumors compared to standard MRI methods. The study will involve up to 5 patients at the University of Maryland, Baltimore, who have suspected infiltrating gliomas or a history of such tumors and are scheduled for surgery. The FDA has approved the use of hyperpolarized 13C-pyruvate in this investigation.

Why it matters

Potential benefit: If successful, this approach could lead to more accurate diagnoses of infiltrating gliomas, potentially improving treatment outcomes.

How similar studies have gone: While this approach is innovative, similar studies using advanced MRI techniques have shown promise in other contexts, suggesting potential for success.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* • Patients with a new brain lesion interpreted as suspected infiltrating gliomas including but not limited to (diffuse astrocytoma WHO grade 2; oligodendroglioma WHO grade 2 and 3; anaplastic astrocytoma WHO grade 3; astrocytoma WHO grade 4), OR, patients with prior history of infiltrating glioma scheduled for surgery for tumor biopsy or resection.

  * Ages 18-80, including male and female
  * Suitable to undergo contrast-enhanced MRI
  * Negative serum pregnancy test

Exclusion Criteria:

* Inability to undergo MRI scan
* Inability to receive IV contrast secondary to severe reaction or renal insufficiency.

Where it's running

  • Rosy Njonkou Tchoquessi
    Baltimore, Maryland, United States
    Recruiting

Study contacts

  • Principal investigator: Dirk Mayer, Dr. rer. nat — University of Maryland, Baltimore
  • Study coordinator: Rosy Njonkou Tchoquessi
  • Email: rnjonkou@som.umaryland.edu
  • Phone: 4107066445

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.