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Clinical Trial Summary

To evaluate efficacy and safety profile of DC bead® TACE in patients with hepatocellular carcinoma in Taiwan.


Clinical Trial Description

To evaluate efficacy and safety profile of DC bead TACE in patients with hepatocellular carcinoma in Taiwan.

This is a multi-center, retrospective, single arm study to explore safety and efficacy of DC bead TACE in hepatocellular carcinoma (HCC) in Taiwan

Retrospective analysis of medical records of all patients who underwent DC Bead TACE at National Taiwan University Hospital, National Cheng Kung University Hospital, and Taichung Veterans General Hospital from 2010-2017/7.

All statistical data were analyzed with SPSS software (SPSS, IBM North America, New York, NY, USA). Demographic and baseline lab data are presented by using descriptive statistics Student's t-test. Survival analysis will includes all patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03283956
Study type Observational
Source National Taiwan University Hospital
Contact Chien-Hung Chen, MD
Phone 886-2-23123456
Email chenhcc@ntuh.gov.tw
Status Not yet recruiting
Phase N/A
Start date September 13, 2017
Completion date August 31, 2018

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