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A Prediction Model of Liver Tumor Recurrence after Ablation Based on the Co-registration of Preoperative Magnetic Resonance Imaging and Intraoperative Computed Tomography

A Prediction Model of Liver Tumor Recurrence after Ablation Based on the Co-registration of Preoperative Magnetic Resonance Imaging and Intraoperative Computed Tomography

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086392
Enrollment
Unknown
Registered
2024-07-01
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

liver cancer

Interventions

experimental group:Thermal ablation therapy

Sponsors

Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Age 18-75 years old, no gender limitation; 2) Liver malignant tumors confirmed by pathology or consistent with clinical diagnosis, including primary liver cancer and metastatic liver cancer; 3) The lesions to be ablated that can be evaluated by imaging: diameter =4cm, number =3; 4) The patient cannot tolerate surgical resection or refuses surgical resection; 5) Child-Pugh A or B, ECOG-PS score =2, expected survival time greater than 3 months.

Exclusion criteria

Exclusion criteria: 1) Child-Pugh C, severe jaundice, especially obstructive jaundice; 2) Diffuse liver cancer, or combined with portal vein trunk to secondary branch or hepatic vein tumor thrombus; 3) Significant liver atrophy, excessive tumor volume, and ablation area needs to reach one-third of the liver volume; 4) With multiple metastases, the expected survival time is less than 3 months; 5) Esophageal ( gastric fundus ) variceal bleeding occurred within 1 month recently; 6) Severe liver, kidney, heart, lung, brain and other major organ function failure; 7) Active infection, especially inflammation of the biliary system; 8) Uncorrectable coagulopathy and severe hematologic abnormalities, with a severe bleeding tendency; 9) Persistent and large amount of ascites, pleural effusion or cachexia; 10) Pregnancy, disturbance of consciousness or unable to cooperate with the treatment; 11) Participated in other clinical studies in the past and are still in the follow-up period; 12) Researchers believe that there are any other factors that are not suitable for enrollment or affect the participation of subjects in the study.

Design outcomes

Primary

MeasureTime frame
Ablation margin in preoperative abdominal enhanced MRI and immediate postoperative abdominal enhanced CT fusion images;Local tumor recurrence assessment in postoperative abdominal enhanced MRI;

Secondary

MeasureTime frame
Local control rate 6 months after ablation (LCR);Progression-free survival 6 months after ablation (PFS);Overall survival 6 months after ablation (OS);

Countries

China

Contacts

Public ContactXiaoyi Ding

Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

dxy10456@rjh.com.cn+86 189 1776 2068

Outcome results

None listed

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