Not yet recruitingNot applicableNCT07480382
Safety and Efficacy of LVD + C-TACE + Tis/Len for Unresectable Right-Liver HCC
Studying Adult hepatocellular carcinoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Hong Wu
- Principal Investigator
- Hong Wu, M.D., Ph.D.West China Hospital
- Intervention
- Liver Venous Deprivation (LVD)(procedure)
- Enrollment
- 30 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2026 – 2028
Study locations (1)
- West China Hospital, Sichuan University, Chengdu, Sichuan, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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