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Clinical Application of Artificial Intelligence Technology Based on ICG Fluorescence Navigation in Laparoscopic Liver Cancer Resection with Microvascular Invasion

Clinical Application of Artificial Intelligence Technology Based on ICG Fluorescence Navigation in Laparoscopic Liver Cancer Resection with Microvascular Invasion

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036557
Enrollment
Unknown
Registered
2020-08-24
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-14

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

Conditions

Hepatocellular carcinoma

Interventions

experimental group:ICG fluorescence assisted laparoscopic radical liver resection
control group:laparoscopic radical resection.

Sponsors

Eastern Hepatobiliary Surgery Hospital, Second Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Ages between 20 to 70, regardless of gender; 2. The primary liver tumor can be resected. Tumors are far from the first, second, and third hepatic portals. Tumors are mainly located in segments II, III, IVb, V, VI, and VIII of the liver. Diameter of the tumors are less than 5cm. 3. Preoperative evaluation of patients with a high risk of MVI (Feng Shen, et al. JAMA Surg, 2016); 4. Liver function Child A, kidney function and cardiopulmonary function are basically normal. Hb >= 90g/L, white blood cell >= 3.0 x 10^9/L, neutrophil count >= 1.5 x 10^9/L, platelet count >= 60 x 10^9/L; 5. No pregnancy, no HCV, HIV or syphilis infection. Patients can understand the situation of this study and have signed the informed consent.

Exclusion criteria

Exclusion criteria: 1) Those who have received chemotherapy, radiotherapy, biological therapy, or other drugs before joining the group; 2) Tumor diameter > 5cm; 3) The tumor has metastasized to other organs, such as lung, brain, bone, etc. 4) Those with obvious surgical contraindications such as renal and cardiopulmonary failure, or those are not suitable for participating in this trial for other reasons.

Design outcomes

Primary

MeasureTime frame
Disease free survival;

Secondary

MeasureTime frame
overall survival;?????;liver function after surgery;Hospital stay;

Countries

China

Contacts

Public ContactWeixing Guo

Eastern Hepatobiliary Surgery Hospital, Second Military Medical University

weixingg88@126.com+86 13918589919

Outcome results

None listed

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