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Contrast Enhanced Ultrasound in Neurosurgery to Improve Glioma Visualization and Border Demarcation

Contrast Enhanced Ultrasound in Neurosurgery to Improve Glioma Visualization and Border Demarcation

Recruiting
18-95 years
All
Phase 0

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Overview

This study plans to learn more about using contrast enhanced ultrasound (CEUS) in brain tumor surgery.

The goal of glioma brain tumor surgery is to remove as much of the glioma as possible. Tumor tissue that is close to normal brain tissue can look very similar. This can make it difficult for the surgeon to remove all the tumor. In this study, we hope to learn if using CEUS during brain tumor surgery will allow the brain surgeon to better see and remove all the tumor tissue.

Eligibility

Inclusion Criteria:

  • Able to sign and date the consent form
  • Stated willingness to comply with all study procedures and be available for the duration of the study
  • Be a male or female aged 18-95
  • Have a planned standard of care surgery for presumed primary or known recurrent glioma
  • WHO performance status \</= 2 (equivalent Karnofsky Performance Status, KPS\>/= 70)
  • Patient of childbearing potential must have a negative pregnancy test within 14 days of inclusion

Exclusion Criteria:

  • Patient at high risk of surgical site infection (e.g., 2 or more previous craniotomies/neurosurgery within the last 3 months, poor skin condition, and/or previously infected surgical field, or any other condition that is of increased infectious risk in the opinion of the neurosurgeon)
  • Known history of hypersensitivity reactions to perflutren lipid microsphere components or to any of the inactive ingredients in the contrast agent.
  • Patient with known or suspected active or chronic infections.
  • Patient with known significant cardiac disease, known to have right-to-left shunts, severe pulmonary hypertension (pulmonary artery pressure \> 90 mm Hg), uncontrolled systemic hypertension, or adult respiratory distress syndrome.
  • Pregnant, or breastfeeding patient.
  • Patient with known sickle cell disease.
  • Any other serious patient medical or psychological condition that may interfere with adequate and safe delivery of treatment and care.
  • Patients under guardianship, curatorship, under legal protection or deprived of liberty by an administrative or judicial decision.

Study details
    Glioma (Any Grade) in the Brain
    Glioma

NCT07050836

University of Colorado, Denver

1 February 2026

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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