Study on Using Contrast Enhanced Ultrasound to Check Treatment Response in Liver Tumor Patients
Sponsor: john eisenbrey
ClinicalTrials ID:NCT06261814
This clinical trial is testing a new way to use ultrasound with a special contrast agent to see how well liver tumors respond to a treatment called transarterial chemoembolization (TACE). This method might allow doctors to evaluate the treatment's effectiveness sooner and more affordably than current methods.
Patient Parameters
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Program Overview
The purpose of this study is to see if a special type of ultrasound, called contrast-enhanced ultrasound (CEUS), can effectively show how liver tumors respond to a treatment known as transarterial chemoembolization (TACE). TACE is a procedure where doctors inject a mixture of chemotherapy and a blocking agent directly into the liver to treat cancer. Currently, doctors use MRI or CT scans to check how well the treatment worked, but these are done 1-2 months after the procedure. CEUS uses sound waves and a contrast agent called Lumason to create images of the liver and can be done during the TACE procedure, potentially allowing for earlier assessment of the treatment's success.
Description
The main goal of this study is to find out how well contrast-enhanced ultrasound (CEUS) can detect changes in liver tumors after they have been treated with transarterial chemoembolization (TACE). Researchers want to see if CEUS can accurately show whether the treatment is working by looking at the blood flow in the tumors.
Secondary goals include:
- Checking if CEUS can spot any remaining active tumor areas during the TACE procedure, so doctors can treat them right away if needed.
- Exploring new imaging techniques to improve CEUS's ability to identify any remaining cancer cells after TACE.
- Seeing if CEUS done before TACE can help predict how well the treatment will work by analyzing the tumor's blood vessels.
In this study, patients will receive an injection of a contrast agent called Lumason and undergo CEUS at different times: 2 weeks before TACE, during TACE, 1-2 weeks after TACE, and 1-2 months after TACE. After the study treatment, patients will have a follow-up visit at 6 months.
Eligibility Criteria
Inclusion Criteria
- Scheduled to receive TACE treatment for a liver tumor
- At least 18 years old
- Medically stable
- Women of childbearing age must have a negative pregnancy test
- Must have signed a consent form agreeing to participate in the study
Exclusion Criteria
- Medically unstable, seriously or terminally ill, or have an unpredictable medical condition
- Known allergies to the components of Lumason
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Sidney Kimmel Cancer Center at Thomas Jefferson University | 19107 | Philadelphia | Pennsylvania |
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