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The effect of Chaihu-Huaji decoction on postoperative syndrome of TACE and the influence of inflammatory factors on primary liver cancer

The effect of Chaihu-Huaji decoction on postoperative syndrome of TACE and the influence of inflammatory factors on primary liver cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047962
Enrollment
Unknown
Registered
2021-06-28
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-03-07

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

Conditions

Primary liver cancer

Interventions

Sponsors

Chongqing Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Those who meet the above-mentioned Western medicine diagnostic criteria for primary liver cancer and TCM syndrome differentiation; 2. Patients with CNLC stage Ib-IIIa; 3. Have not received any treatment for HCC, such as surgical resection, ablation, TACE, etc.; 4. Those who have good compliance, take medicine on time, review at the specified time, and have a cheerful personality; 5. Patients between the ages of 18 and 70; 6. The choice of embolic agent is ultra-liquefied lipiodol, and the dosage is determined according to the size of the tumor. The maximum amount of one administration does not exceed 20ml.

Exclusion criteria

Exclusion criteria: 1. Combined with other systemic malignant tumors at the same time; 2. Serious adverse drug reactions; 3. Combined with severe complications of advanced decompensation of tumor and liver cirrhosis, such as upper gastrointestinal bleeding, hepatorenal syndrome, hepatic encephalopathy, etc.; 4. Those who are mentally ill or unable to cooperate; 5. There are absolute contraindications to TACE treatment; 6. Patients with severe heart disease, or kidney, brain, lung and hematopoietic system diseases; 7. The researcher believes that it is not suitable to participate in this clinical researcher.

Design outcomes

Primary

MeasureTime frame
Blood routine;Liver function;C-reactive protein;Alpha-fetoprotein;IL-12;Basic fibroblast growth factor;Vascular endothelial growth factor;MMP-9;

Countries

China

Contacts

Public ContactHuang Yi

Chongqing Traditional Chinese Medicine Hospital

417094299@qq.com+86 13637808573

Outcome results

None listed

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