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
| Type | Name | Description |
|---|---|---|
| DRUG | TACE combined with Acoradine | Transcatheter 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.