TACE Combined With Synchronous Radiofrequency /Microwave Ablation to Treat Large and Huge Hepatocellular Carcinoma

NCT02630108 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 280

Last updated 2016-10-18

No results posted yet for this study

Summary

It is a prospective and multi-center clinical research in China to compare the efficacy, safety and related impact factors between TACE alone and TACE combined with synchronous multi-point MWA/RFA for large and huge liver cancer.

Conditions

  • Carcinoma, Hepatocellular

Interventions

PROCEDURE

Thermal Ablation

Thermal ablation in this trial includes radiofrequency ablation and microwave ablation, one of them can be chosen to be performed.

DRUG

EADM

EADM is a chemotherapy drug used in transarterial chemoembolization (TACE).Dosage: EADM 30-60 mg per patient,depending on the situation of the patient.

DRUG

Ultra-fluid lipiodol

Ultra-fluid lipiodol is a kind of embolization material used in TACE. Standard: 38% ultra-fluid lipiodol .

OTHER

Gelatin sponge articles

Gelatin sponge articles embolization material used in TACE. Standard: 350-560 um in diameter.

Sponsors & Collaborators

  • Xijing Hospital

    collaborator OTHER
  • Changhai Hospital

    collaborator OTHER
  • Eastern Hepatobiliary Surgery Hospital

    collaborator OTHER
  • Shanghai Cancer Hospital, China

    collaborator OTHER
  • Shengjing Hospital

    collaborator OTHER
  • The Third Affiliated Hospital of Harbin Medical University

    collaborator OTHER
  • Jilin Provincial Tumor Hospital

    collaborator OTHER
  • Zhejiang Cancer Hospital

    collaborator OTHER
  • Jiangsu Cancer Institute & Hospital

    collaborator OTHER
  • Guangdong Provincial People's Hospital

    collaborator OTHER
  • Sichuan Cancer Hospital and Research Institute

    collaborator OTHER
  • Henan Cancer Hospital

    collaborator OTHER_GOV
  • Anhui Provincial Hospital

    collaborator OTHER_GOV
  • The First Affiliated Hospital of Anhui Medical University

    collaborator OTHER
  • Qilu Hospital of Shandong University

    collaborator OTHER
  • Shandong Tumor Hospital

    collaborator OTHER
  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • Chinese PLA General Hospital

    collaborator OTHER
  • Nanfang Hospital, Southern Medical University

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • LanZhou University

    collaborator OTHER
  • Sun Yat-sen University

    collaborator OTHER
  • Hunan Provincial People's Hospital

    collaborator OTHER
  • Affiliated Zhongshan Hospital of Dalian University

    collaborator OTHER
  • Shanghai Zhongshan Hospital

    lead OTHER

Principal Investigators

  • Jianhua Wang, MD · Shanghai Zhongshan Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2015-12-31
Primary Completion
2017-12-31
Completion
2018-04-30

Countries

  • China

Study Locations

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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 NCT02630108 on ClinicalTrials.gov