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Clinical Trials in Taiwan / NCT07178093
Recruiting Not applicable

Effects of Antrodia Cinnamomea on the Hepatoma Patients After Transcatheter Hepatic Artery Chemoembolization

NCT07178093 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2023-01-01
Last updated
2025-09-17

Condition(s) studied

Hepatocellular CarcinomaTransarterial Chemoembolization

Investigational drug(s) / intervention(s)

Antrodia cinnamomeaplacebo

Antrodia cinnamomea: The experiment lasted for 11 days, and patients were required to take Kangjian Antrodia cinnamomea 3 days before embolization, the day of embolization to the 7th day after surgery, once a day in the morning and evening after meals, 2 capsules each time.

placebo: The experiment lasted for 11 days, and patients were required to take placebo 3 days before embolization, the day of embolization to the 7th day after surgery, once a day in the morning and evening after meals, 2 capsules each time.

Study summary

Effects of Antrodia cinnamomea on the hepatoma patients after Transcatheter hepatic artery chemoembolization

Eligibility

Sex
ALL
Min age
20 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Sign the informed consent form * Aged between 20 and 80 * Child-Pugh score class A, B * Serum bilirubin level ≤ 1.5 times the upper limit of normal, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels ≤ 2 times the upper limit of normal Exclusion Criteria: * Unwillingness to sign the informed consent form * Child-Pugh score class C * Patients with main portal vein thrombosis * Patients with diffuse liver tumors * Those who are allergic to the contrast medium * Those with abnormal coagulation function * Those with severe dysfunction of brain, heart and lung * Patients with severe renal dysfunction (except those receiving renal dialysis) * Unable to cooperate * Those with uncontrolled arrhythmia and unstable blood pressure * Some patients with abnormal thyroid function * Any other contraindications such as active gastrointestinal bleeding, refractory ascites, or severe portal hypertension * Pregnant or lactating women

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Taichung Tzu-Chi Hospital Taichung Taiwan Recruiting

More Taichung Tzu Chi Hospital trials in Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07178093 on ClinicalTrials.gov ↗ ← All trials in Taiwan