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Study of alleviating effect and its molecular mechanism of Jiedu Granules on inflammatory reaction after transcatheter arterial chemoembolization in hepatocellular carcinoma

Study of alleviating effect and its molecular mechanism of Jiedu Granules on inflammatory reaction after transcatheter arterial chemoembolization in hepatocellular carcinoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015152
Enrollment
Unknown
Registered
2018-03-10
Start date
2018-03-01
Completion date
Unknown
Last updated
2018-03-12

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

Conditions

Primary Liver Cancer

Interventions

Jiedu Granules:Jiedu Granules
Control Group:Basic treatment

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: (1) Primary liver cancer patients diagnosed according to the criteria for diagnosis and treatment of primary liver cancer (2017 edition); (2) Patients should not receive any Chinese herbal medicine or systemic treatment in the past two weeks; (3) ECOG (Eastern Cooperative Oncology Group) score 0-1; (4) Compensatory liver function, or Child-Pugh grade A or B; (5) The patient needs at least 3 months of life expectancy; (6) Voluntarily to accept the treatment of the study protocol and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Taking other drugs that may affect the evaluation of observational indicators during the trial period; (2) The Child-Pugh score of liver function was grade C; (3) WBC <2.0×10^9/L, platelets <30×10^9/L; (4) The ratio of tumors to whole liver is greater than 70%; (5) Combining severe primary diseases such as cardiovascular, hepatic, renal and hematopoietic diseases and psychotic patients; (6) The enrolled patients do not use treatment drugs according to our project, or it is impossible to judge the curative effect, or incomplete data, etc. that affect the efficacy judgment.

Design outcomes

Primary

MeasureTime frame
Inflammatory factors;

Secondary

MeasureTime frame
Liver function;Routine blood test;

Countries

China

Contacts

Public ContactBinbin Cheng

Shanghai Changhai Hospital

cbb8202@126.com+86 13916943770

Outcome results

None listed

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