Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01327521

Transarterial Chemoembolization vs CyberKnife for Recurrent Hepatocellular Carcinoma

International Randomized Study of Transarterial Chemoembolization Versus CyberKnife for Recurrent Hepatocellular Carcinoma

Status
Withdrawn
Phase
Phase 3
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Albert Koong · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Primary Objective: To compare the efficacy of TACE vs. CyberKnife SBRT in the treatment of locally recurrent HCC after initial TACE. Secondary Objectives: 1. To determine the progression-free survival of TACE vs. CyberKnife SBRT 2. To determine the overall survival of TACE vs. CyberKnife SBRT for locally recurrent HCC 3. To determine the toxicities associated with TACE or CyberKnife SBRT for the treatment of recurrent HCC.

Conditions

Interventions

TypeNameDescription
DEVICECyberKnifeStandard of Care
PROCEDURETACEStandard of Care
DRUGCT ContrastStandard of Care
DRUGdoxorubicinStandard of Care
DRUGEpirubicinStandard of Care
DRUG5-fluorouracilStandard of Care
DRUGMitomycin CStandard of Care
DRUGGemcitabineStandard of Care
DRUGCisplatinStandard of Care
DEVICESMANCSStandard of Care

Timeline

Start date
2011-02-01
Primary completion
2014-02-01
First posted
2011-04-01
Last updated
2012-06-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01327521. Inclusion in this directory is not an endorsement.