RecruitingPhase 2NCT06261814

Contrast Enhanced Ultrasound to Evaluate Response to Chemoembolization in Patients With Liver Tumors

2D and 3D Contrast Enhanced Ultrasound of Chemoembolization


Sponsor

john eisenbrey

Enrollment

266 participants

Start Date

Aug 7, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This phase II trial evaluates the diagnostic performance of contrast-enhanced ultrasound (CEUS) for assessing treatment response in patients undergoing transarterial chemoembolization (TACE) for liver tumors. TACE is a hepatic artery embolization technique involving the injection of a blocking agent and a chemotherapy agent to treat liver cancers. Currently, contrast enhanced magnetic resonance imaging or computed tomography are used to assess disease response 1-2 months after TACE treatment, but ultrasound may be a less expensive, earlier alternative. CEUS is an imaging procedure that uses high-frequency sound waves to generate images of the body after administering Lumason, an imaging agent used to enhance visualization of blood flow on ultrasounds. CEUS is able to be performed during the TACE procedure, making it possible to evaluate treatment response earlier than standard techniques. CEUS may be an effective method to evaluate treatment response more accurately and much earlier than current standard evaluation methods.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is using a special type of ultrasound imaging called contrast-enhanced ultrasound (CEUS) to evaluate how well a procedure called chemoembolization (TACE) — where chemotherapy is delivered directly into liver tumor blood vessels — is working in patients with liver tumors. **You may be eligible if...** - You are at least 18 years old - You are scheduled to receive TACE treatment for a liver tumor - You are medically stable - You have signed informed consent - If you are a woman of childbearing age, you have a negative pregnancy test **You may NOT be eligible if...** - You are medically unstable, seriously ill, or terminally ill - You have a known allergy or sensitivity to the ultrasound contrast agent (Lumason) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSulfur Hexafluoride Lipid Microspheres

Given IV

PROCEDUREContrast-Enhanced Ultrasound

Undergo CEUS

PROCEDURETransarterial Chemoembolization

Undergo TACE

OTHERMedical Chart Review

Ancillary studies


Locations(1)

Sidney Kimmel Cancer Center at Thomas Jefferson University

Philadelphia, Pennsylvania, United States

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NCT06261814


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