Blood Volume Assessment of Hepatocellular and Metastatic Carcinomas in the Liver

NCT02288910 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 7

Last updated 2020-10-08

No results posted yet for this study

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.

Conditions

Sponsors & Collaborators

  • Rush University Medical Center

    lead OTHER

Principal Investigators

  • Mark Supanich, PH.D. · Rush University Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2019-07-31
Completion
2020-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02288910 on ClinicalTrials.gov