Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06644937

Single-arm Clinical Trial of TACE in Combination With Icaritin as Adjuvant Therapy After Surgery in Patients With Hepatocellular Carcinoma at High Risk of Recurrence

Status
Recruiting
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Zhujiang Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

To assess 1-year recurrence-free survival (RFS) in patients with hepatocellular carcinoma (HCC) who are at high risk of Inguinal orchiectomy recurrence usingTACE combined with icaritin

Conditions

Interventions

TypeNameDescription
DRUGTACE combined with AcoradineTranscatheter hepatic arterial chemoembolization (TACE) : the treatment interval was 28 days, the window period was ± 7 days. Subjects received a maximum of 4 TACE treatments; reduced and delayed treatment: laboratory tests were performed before the start of each cycle of TACE, with investigator criteria confirming whether TACE treatment was feasible. Acoradine: 6 tablets bid, taken after meals for 6 months or until intolerable or progressive disease (starting one month after surgery) .

Timeline

Start date
2024-11-29
Primary completion
2026-10-31
Completion
2026-12-31
First posted
2024-10-16
Last updated
2025-09-23

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06644937. Inclusion in this directory is not an endorsement.