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Clinical Trial Summary

To analyze specific angiogenic, inflammatory and immune profiles in hepatocellular carcinoma patients who undergo radioembolization.


Clinical Trial Description

Patients who have planned lobar radioembolization (TheraSphere (TS)) and consent to this study will have peripheral blood samples collected pre-TS, post-TS, 4 hours post-TS, 24 hours post-TS, 3 days post-TS, 7 days post-TS and 30 days post-TS to analyze specific angiogenic, inflammatory and immune profiles. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03203837
Study type Observational
Source Northwestern University
Contact
Status Terminated
Phase
Start date July 5, 2017
Completion date January 6, 2020

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