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Evaluation of curative effect of TCM Tiaogan Lipi approach in the prevention and treatment of primary liver cancer after Transcatheter arterial chemoembolization

Evaluation of curative effect of TCM Tiaogan Lipi approach in the prevention and treatment of primary liver cancer after Transcatheter arterial chemoembolization

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008036
Enrollment
Unknown
Registered
2016-04-09
Start date
2016-05-20
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma

Interventions

test team:TACE+ Chinese medicine granule
control group:TACE+placebo

Sponsors

Beijing Hospital of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. With the western medicine, Chinese medicine diagnosis of primary hepatocellular carcinoma; 2. Meet the indications for TACE; 3. Stage II or III; 4. Unable or unwilling to accept surgical treatment or surgical treatment of incomplete or recurrence; Using Child-Pugh improved liver function classification, liver function rating of A or B; 5. The liver function was improved by Child-Pugh classification method, and the liver function was rated as A or B. 6.According to the The guiding principle of clinical research on new drugs" determinant for liver stagnation and spleen deficiency; 7. Aged 18-75; 8. The function of the important organs such as heart and kidney is normal; 9. The ECOG score of 0-2, the expected survival time more than 3 months; 10.Preoperative patients based on image science data measured tumor size. If the lesion was solitary and maximum tumor diameter greater than or equal to 5 cm; if multiple lesions, multiple maximum lesion diameter and greater than or equal to 5cm. 11. Signed informed consent, voluntary subjects.

Exclusion criteria

Exclusion criteria: 1. Metastatic liver cancer; 2. Bile duct carcinoma with clear pathological diagnosis; 3. Having TACE treatment contraindications; 4. Having similar symptoms like PES before TACE; 5. With serious heart, kidney and hematopoietic system of primary disease or mental disorder or having serious complications such as liver failure, upper gastrointestinal bleeding in prior TACE; 6.gestation or lactating; 7. participating other clinical drug experimental group;

Design outcomes

Primary

MeasureTime frame
symptom;liver function;

Secondary

MeasureTime frame
TCM syndrome integral;Physical fitness evaluation;

Countries

China

Contacts

Public ContactGuowang Yang
guowang_yang@163.com+86 13701116943

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026