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Research and application of GPS magneto-guided conformal microwave ablation system in solid tumor ablation

Research and application of GPS magneto-guided conformal microwave ablation system in solid tumor ablation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081847
Enrollment
Unknown
Registered
2024-03-13
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Hepatocellular Carcinoma

Interventions

Treatment group:Ablation treatment for patients with hepatocellular carcinoma with the guidance of GPS magnetic navigation

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: ? The maximum diameter of the tumor is 3-5cm and the number of lesions is less than 3; ? Age= 18 years old; ? HCC with clinical diagnosis or pathological diagnosis in accordance with the Guidelines for the Diagnosis and Treatment of Primary Liver Cancer; ? The general condition of the patient was good, the physical status score (PS) was 0-1, and without obvious organic lesions of the heart, lungs, kidneys and other important organs; ? Liver function belongs to Child-Pugh class A or B; ? No extrahepatic metastasis and vascular invasion.

Exclusion criteria

Exclusion criteria: 1) Patients with other uncured malignancies in the past (within 5 years) or at the same time;2) Aminotransferase (AST or ALT) > 5 times the normal value and/or the total bilirubin is significantly elevated >3 times the normal value;3) Patients with severe infection, fever, bleeding tendency, refractory ascites effusion, and stage III and IV hepatic encephalopathy;4) Severe heart, lung, and kidney diseases, cerebrovascular accidents, Patients with severe diabetic complications, 5) pregnant or lactating patients, patients with mental disorders, 6) allergies, or known allergies to contrast agents and antibiotics, 7) those who are participating in clinical trials of other drugs or receiving other traditional Chinese medicine treatments, 8) Those who are using systemic therapy, 9) Those who are considered by the investigator to be unsuitable for clinical trials for other reasons (such as those with active alcoholic cirrhosis or autoimmune liver disease)

Design outcomes

Primary

MeasureTime frame
complete response rate;

Secondary

MeasureTime frame
objective response rate;disease control rate;Changes in serum tumor markers;safety assessment;

Countries

China

Contacts

Public ContactLiu Lingxiao

Zhongshan Hospital, Fudan University

liulingxiao2022@163.com+86 186 1688 1019

Outcome results

None listed

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