Combined Treatment of RFA and Sorafenib on Recurrent HCC

NCT01470495 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 430

Last updated 2017-03-28

No results posted yet for this study

Summary

RFA is a routaine treatment of recurrent HCC. Recently Sorafenib was reported to be a promising drug to treat late stage HCC. But few studies were related with its effectiveness on recurrent HCC. So the investigators hypothesized that combined RFA and Sorafenib might reduce the frequency of recurrence and improve the overall survival and disease free survial.

Conditions

  • HCC
  • Radiofrequency Ablation
  • Sorafenib

Interventions

OTHER

RFA + Sorafenib

combined RFA and Sorafenib to treat recurrent HCC

OTHER

RFA

treat Recurrent HCC with RFA

Sponsors & Collaborators

  • Hunan Province Tumor Hospital

    collaborator OTHER
  • Tang-Du Hospital

    collaborator OTHER
  • Xijing Hospital

    collaborator OTHER
  • First Affiliated Hospital of Guangxi Medical University

    collaborator OTHER
  • First Affiliated Hospital Xi'an Jiaotong University

    collaborator OTHER
  • Anhui Provincial Hospital

    collaborator OTHER_GOV
  • Xiangya Hospital of Central South University

    collaborator OTHER
  • Xinqiao Hospital of Chongqing

    collaborator OTHER
  • Xinjiang Tumor Hospital

    collaborator UNKNOWN
  • People's Hospital of Guangxi Zhuang Autonomous Region

    collaborator OTHER
  • Henan Cancer Hospital

    collaborator OTHER_GOV
  • People's Hospital of Sichuan

    collaborator UNKNOWN
  • Huaxi Hospital

    collaborator OTHER
  • Southwest Hospital, China

    lead OTHER

Principal Investigators

  • Kuansheng Ma, MD,Ph.D · Southwest Hopstial

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01470495 on ClinicalTrials.gov