Clinical Trials Directory

Trials / Completed

CompletedNCT02288910

Blood Volume Assessment of Hepatocellular and Metastatic Carcinomas in the Liver

Status
Completed
Phase
Study type
Observational
Enrollment
7 (actual)
Sponsor
Rush University Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This project investigates the feasibility of assessing the relative blood volume of carcinomas in patients with Hepatocellular Carcinoma (HCC) and liver metastases from pancreatic or colorectal cancer compared to normal liver from DynaCT acquisitions on an interventional platform.

Detailed description

This project will enroll patients with non-diffuse liver disease who are candidates for chemo or radioembolization to treat or manage the disease during an image guided intervention. Subjects will undergo a CT perfusion study of the liver prior to the radioembolizaiton mapping procedure or prior to the chemoembolization treatment. During the radioembolization mapping or chemoembolization procedure, 2 DynaCT acquisitions on the interventional C-arm will be acquired (the second during an injection of an iodinated contrast material) and will be processed using Siemens' PBV software to generate blood volume maps. The diagnostic accuracy of the two approaches to assess the vascularity of the tumors will be assessed.

Conditions

Timeline

Start date
2014-11-01
Primary completion
2019-07-01
Completion
2020-07-01
First posted
2014-11-11
Last updated
2020-10-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02288910. Inclusion in this directory is not an endorsement.