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A homogeneous lipiodol formula based on pure nano-ICG is used for precise surgical navigation after long-term embolization of giant liver cancer

A homogeneous lipiodol formula based on pure nano-ICG is used for precise surgical navigation after long-term embolization of giant liver cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058803
Enrollment
Unknown
Registered
2022-04-17
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Liver Cancer

Interventions

NanoICG Group:Interventional embolization with pure drug nano ICG lipiodol suspension

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. The age of patients is 18-60 years old, and the life expectancy is >= 3 months; 2. Patients with primary hepatocellular carcinoma confirmed by histology or cytology or meeting the clinical diagnostic criteria (basic chronic liver disease, typical imaging features, AFP changes) of the code for the diagnosis and treatment of primary liver cancer (2019 Edition) issued by the Health Commission; 3. BCLC stage is stage B or C (surgical resection or surgical resection with large injury, liver transplantation and local ablation are not suitable); 4. Single or multiple lesions in the liver are located in the half liver or limited to the adjacent three liver lobes; 5. The primary branch of portal vein of at least one leaf is unobstructed; 6. The liver function is child-a or child-b before surgical resection, and can reach child-a after liver protection, nutritional rehydration and other treatment; 7. Eastern United States cancer cooperation group status score (ECoG PS) = white blood cell count >= 3.0*10^9/L, 350*10^9/L >= platelet count >= 50*10^9/L, Prothrombin time (PT) shall not exceed the upper limit of normal control for 3 seconds; Serum creatinine was less than 1.5 times of the upper limit of normal; Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were less than 3 times of the upper limit of normal; 9. Inform the patients of the possible advantages and disadvantages before and after the operation in detail, and the patients and their families voluntarily choose the treatment plan and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Recurrent liver cancer or previous treatment of liver cancer or portal vein tumor thrombus (including surgery, external radiotherapy, molecular targeted drugs, local ablation, Tai / Tae / TACE, etc.) 2. The tumor thrombus extends into the superior mesenteric vein and/or splenic vein; And patients with hepatic vein, hepatic segment inferior vena cava tumor thrombus or extrahepatic metastasis; 3. Patients with other malignant tumors; 4. Serious heart, lung, kidney, brain, and other important organ diseases; 5. Contraindications of TAE: diffuse liver cancer or tumor volume accounting for 70% or more of the whole liver, intractable massive ascites, intrahepatic high flow arteriovenous shunt; Total bilirubin > 51umol / L and/or albumin < 28g / L, which can not be improved after symptomatic treatment; Combined with active infection, especially bile duct inflammation; Female patients are pregnant or lactating.

Design outcomes

Primary

MeasureTime frame
R0 resection rate;Operation time;Bleeding volume;Time of clamping porta hepatis;Progression-free survival;

Countries

China

Contacts

Public ContactJingdong Li

Affiliated Hospital of North Sichuan Medical College

Li-Jingdong@hotmail.com+86 18882319097

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026