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Clinical Trial Summary

The primary aim of this trial is to estimate the duration of hepatic progression-free survival (HPFS) in participants treated with bland embolization (BE), transcatheter arterial Lipiodol chemoembolization (TACE), and embolization by drug-eluting beads (DEB). The primary hypothesis is that chemoembolization will be nearly twice as durable as bland embolization; thatis, the hazard ratio for HPFS will be 1.76 or better.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02724540
Study type Interventional
Source Abramson Cancer Center at Penn Medicine
Contact
Status Active, not recruiting
Phase Phase 2
Start date March 2016
Completion date September 2024

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