Impact of C-arm CT in Patients With HCC Undergoing TACE: Optimal Imaging Guidance
Carcinoma, Hepatocellular

About this trial
This is an interventional diagnostic trial for Carcinoma, Hepatocellular
Eligibility Criteria
Inclusion Criteria:
Patients must be affected by HCC
Patients must be 18 years old or older
Patients must have received an abdominal CT, PET/CT scan or MRI, completed prior to the TACE procedure.
Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
Subjects under the age of 18
Pregnant women
Sites / Locations
- Stanford University School of Medicine
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
C-arm CT + DSA as needed'
DSA only
In the group of subjects randomized in this group, the image guidance component of the procedure will be conducted by the acquisition of 3D CT-like images during a trans-hepatic arterial injection of iodinated contrast agent for road mapping the tumor feeding vessels and supplemented by DSA as needed by the operating physician as imaging guidance for planning tumor(s) treatment approach.
In the group of subjects randomized in this group, present standard of care, i.e DSA imaging only will be used by the operating physician to map out the tumor vessels and used for treatment approach. Additional 3D CT-like images will be obtained, but only used if the operator cannot perform adequate planning using DSA alone.