Hepatocellular Carcinoma Clinical Trial
Official title:
The Safety and Efficacy Evaluation of XSLJZ in Advanced Hepatocellular Carcinoma Patients With Multiple Protein Kinase Inhibitor Therapy: A Randomized, Double-Blind, Controlled Trial
Verified date | May 2024 |
Source | China Medical University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the study was search the safety and efficacy of the of Xiang Sha Liu Jun Zi Decoction (XSLJZ) in advanced hepatocellular carcinoma patients with multiple protein kinase inhibitor therapy. Evaluate the treatment effect on the symptoms of appetite and quality of life in advanced hepatocellular carcinoma patients
Status | Completed |
Enrollment | 10 |
Est. completion date | May 30, 2023 |
Est. primary completion date | December 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 75 Years |
Eligibility | Inclusion Criteria: 1. Advanced hepatocellular carcinoma patient 2. use multiple protein kinase inhibitor therapy paid by National Health Care Insurance system (NHCIS) in Taiwan 3. Child-Pugh A class 4. Eastern Cooperative Oncology Group performance status of 0-2 5. survival period over 3 months 6. used Xiang Sha Liu Jun Zi Decoction for one month before the multiple protein kinase inhibitor therapystarting point Exclusion Criteria: 1. combine other cancer at the same time 2. ESRD under dialysis 3. heart disease,CHF?CAD?arrhythmia?hypertension (SBP>150mmHg,DSP>90 mmHg) 4. current serious infection 5. GI bleeding within 30 days 6. receive organ transplant 7. Child-Pugh Class B or C liver status? 8. Refractory Ascites in Liver Cirrhosis |
Country | Name | City | State |
---|---|---|---|
Taiwan | China Medical University hospital | Taichung | ??? |
Lead Sponsor | Collaborator |
---|---|
China Medical University Hospital |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | body weight | patient body weight | 8 weeks | |
Primary | EORTC QLQ-C30 score | European Organization for Research and Treatment of Cancer Core Quality of Life Questionnaire score | 8 weeks | |
Primary | EORTC QLQ-HCC18 | European Organization for Research and Treatment of Hepatocellular carcinoma Core Quality of Life Questionnaire score | 8 weeks | |
Primary | CASQ | cancer appetite and symptom questionnaire | 8 weeks | |
Primary | FACT-G | Functional Assessment of Cancer Therapy - General | 8 weeks | |
Secondary | CCMQ | Chinese medicine questionnaire | 8 weeks | |
Secondary | tong diagnosis | tong diagnosis by Automatic Tongue Diagnosis System | 8 weeks | |
Secondary | pulse diagnosis | pulse diagnosis by Huang's Sphygmography in Frequeny-domained Parameters | 8 weeks |
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