Clinical Trials Directory

Trials / Unknown

UnknownNCT02018757

Safety and Efficacy of Arsenic Trioxide Contained in TACE in the Treatment of HCC

Clinical Application Study of Transarterial Chemoembolization Containing Arsenic Trioxide in the Treatment of Hepatocellular Carcinoma

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
250 (estimated)
Sponsor
First Hospital of China Medical University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to determine whether transarterial chemoembolization containing arsenic trioxide is safe and effective in the treatment of intermediate-stage hepatocellular carcinoma.

Conditions

Interventions

TypeNameDescription
DRUGTACE containing As2O3transarterial chemoembolization containing a mixture of 20mg of arsenic trioxide, 40mg of adriamycin and some dose of 40% ultra-fluid lipiodol
DRUGTACE containing placebotransarterial chemoembolization containing a mixture of 20mg of placebo, 40mg of adriamycin and some dose of 40% ultra-fluid lipiodol

Timeline

Start date
2014-01-01
Primary completion
2015-12-01
First posted
2013-12-23
Last updated
2014-05-28

Locations

5 sites across 1 country: China

Source: ClinicalTrials.gov record NCT02018757. Inclusion in this directory is not an endorsement.