Actively Recruiting

Phase 1
Age: 19Years +
All Genders
NCT03830151

Hyperpolarized Carbon C 13 Pyruvate in Diagnosing Glioma in Patients With Brain Tumors

Led by M.D. Anderson Cancer Center · Updated on 2026-01-13

13

Participants Needed

1

Research Sites

502 weeks

Total Duration

On this page

Sponsors

M

M.D. Anderson Cancer Center

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This trial studies how an imaging agent, hyperpolarized carbon C 13 pyruvate, works in diagnosing glioma in patients with brain tumors. Giving hyperpolarized carbon C 13 pyruvate before an advanced imaging technique called a magnetic resonance spectroscopic imaging (MRSI) scan may help researchers better diagnose glioma in patients with brain tumors.

CONDITIONS

Official Title

Hyperpolarized Carbon C 13 Pyruvate in Diagnosing Glioma in Patients With Brain Tumors

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Written informed consent obtained from each participant including healthy volunteers
  • Healthy volunteers have no contraindications to MR scanning
  • All patients enrolled in Stereotactic RadPath trial (#2011-0370)
  • Age over 18 years
  • Candidate for cerebral tumor resection with suspected or biopsy-proven primary brain tumor
  • Able to understand and give consent
  • Agree to undergo MRI including perfusion, diffusion, and spectroscopic imaging within 14 days before procedure
  • Glomerular filtration rate (GFR) greater than 60 (or considered for alternate contrast dose if 30-60)
  • Willing to give signed informed consent for C13-Pyruvate MR Spectroscopy
Not Eligible

You will not qualify if you...

  • Unfavorable anatomy preventing safe stereotactic biopsy
  • Presence of pacemakers, electronic stimulation devices, metallic foreign bodies or other MR unsafe implants
  • Pregnancy
  • Claustrophobia not responsive to oral medication
  • Prior brain tumor treatment including surgical resection, radiation, or chemotherapy (previous biopsy allowed)
  • History of cardiac arrhythmia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

M D Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

D

Dawid Schellingerhout

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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