Treatment of Intermediate-stage Hepatocellular Carcinoma

NCT03274427 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2017-09-15

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy and safety of transarterial chemoembolization (TACE) combined with arginine hydrochloride and trimetazidine hydrochloride tablets in the treatment of patients with hepatocellular carcinoma.

Conditions

Interventions

DEVICE

Basic drugs therapy of HCC by TACE

Basic drugs include: 1. Molecular targeted drugs for HCC:apatinib; 2. Antiviral drugs (ETV or TDF) should be given to patients who were infected with HBV or HCV; 3. Patients with liver dysfunction should be treated with conventional hepatoprotective agents drugs (including glycyrrhizin, reduced glutathione, vitamin C,etc); 4. Patients with ascites symptoms should be treated with furosemide and spironolactone according to the urine volume, and they also should be treated with proton pump inhibitors in the prevention of gastrointestinal bleeding; 5. Other basic diseases were treated routinely.

DRUG

Arginine hydrochloride

Arginine hydrochloride injection 5g/dose; 40g/d; ivgtt; sustained medication for 24 days; drug withdrawal for 4 days.

DRUG

Trimetazidine hydrochloride

Trimetazidine hydrochloride, 20mg/tablet, 40mg, twice a day.

Sponsors & Collaborators

  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • Luoyang Central Hospital

    collaborator OTHER
  • Nanyang Central Hospital

    collaborator OTHER
  • Anyang Tumor Hospital

    collaborator OTHER
  • Shenma Medical Group General Hospital

    collaborator OTHER
  • First People's Hospital of Shangqiu

    collaborator OTHER
  • Jiaozuo third people's hospital

    collaborator UNKNOWN
  • The First Affiliated Hospital of Zhengzhou University

    lead OTHER

Principal Investigators

  • Zujiang Yu · The First Affiliated Hospital of Zhengzhou University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2017-07-18
Primary Completion
2021-07-31
Completion
2021-07-31

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 NCT03274427 on ClinicalTrials.gov