RecruitingPhase 2NCT07337421
Efcacy and Safety of Postoperative Adjuvant Hepatic Arterial Infusion Chemotherapy With mFOLFOX in Hepatocellular Carcinoma With High-risk Recurrence Factors
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
- Northern Jiangsu People's Hospital
- Principal Investigator
- Dou-sheng BaiClinical Medical College, Yangzhou University
- Intervention
- mFOLFOX ：Oxaliplatin,leucovorin calcium,5-fluorouracil(drug)
- Enrollment
- 30 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2025 – 2027
Study locations (1)
- Clinical Medical College of Yangzhou University, Yangzhou, Jiangsu, 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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