Overview

Contrast-Enhanced Ultrasound for the Prediction of Bile Duct Cancer Response to Radioembolization Treatment

Status:
Recruiting
Trial end date:
2023-10-31
Target enrollment:
0
Participant gender:
All
Summary
This clinical trial tests whether contrast-enhanced ultrasound can predict the response of bile duct cancer to targeted radiotherapy (radioembolization treatment). Contrast-enhanced ultrasound uses gas microbubbles that may provide enhancement on ultrasound. It is also possible to pop these microbubbles using ultrasound imaging. Tumors that experience popping of these microbubbles may be easier to kill with radiotherapies. Therefore, this trial may also help doctors see if ultrasound-triggered microbubble popping can improve bile duct cancer response to radiotherapy. Another purpose of this trial is to test if the pressure inside the tumor estimated through ultrasound can be used to predict the tumor response to radiotherapy.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Thomas Jefferson University
Criteria
Inclusion Criteria:

- Be scheduled for sub-lobar radioembolization therapy of a previously untreated
intrahepatic cholangiocarcinoma greater than 1 cm but small enough to be fully
visualized in the ultrasound three-dimensional (3D) volume (approximately 6 cm maximum
diameter, but depth dependent)

- Be at least 18 years of age

- Be medically stable

- If a female of child-bearing age, have a negative pregnancy test prior to each
ultrasound exam

- Have signed Informed Consent to participate in the study

Exclusion Criteria:

- Females who are pregnant or nursing

- Patients with recent cerebral hemorrhage

- Patients with known sensitivities to albumin, blood, or blood products

- Patients with known hypersensitivity to perflutren

- Patients with known congenital heart defects

- Patients with severe emphysema, pulmonary vasculitis, or a history of pulmonary emboli

- Patients with bilirubin levels > 2 mg/dL