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A real-world study of the initial use of acoradine in patients with hepatocellular carcinoma after liver transplantation

A real-world study of the initial use of acoradine in patients with hepatocellular carcinoma after liver transplantation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101389
Enrollment
Unknown
Registered
2025-04-24
Start date
2024-07-27
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver transplantation

Interventions

Experimental group:Icaritin combined with TKI

Sponsors

The Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old, male or female; 2. Patients with recurrence of liver cancer after liver transplantation and those with high risk factors after transplantation need drug prevention; 3. Hepatocellular carcinoma meets clinical diagnostic criteria and/or is confirmed by histopathological examination; 4. Contains at least one target lesion whose size and enhanced area can be accurately measured on dynamic enhanced CT or MRI; 5. Subjects were willing to accept Icaritin-based treatment; 6. Subjects volunteered to participate in the project.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. In the clinician's judgment, the patient was not suitable for inclusion in other conditions.

Design outcomes

Primary

MeasureTime frame
PFS;

Secondary

MeasureTime frame
1 year OS rate;Safety;

Countries

China

Contacts

Public ContactWei Rao

The Affiliated Hospital of Qingdao University

qdfy_raowei@qdu.edu.cn+86 186 6180 3090

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026