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

Stopped early · Early Phase 1

Conditions studied: Glioma (Any Grade) in the Brain, Glioma

In brief

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.

Key facts

Study ID

NCT07050836

Run by

University of Colorado, Denver

People needed

2

Starts

2025-12-05

Expected to finish

2026-01-27

Last updated by the study team

2026-06-22

Who can join

Age: 18 and older, up to 95. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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.

Where it is running

• University of Colorado Anschutz Medical Campus — Aurora, Colorado, United States

Full record on ClinicalTrials.gov

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