Skip to content

Indocyanine Green Molecular Fluorescence Imaging Technique Using in Diagnosis and Treatment of Primary Liver Cancer

Multicenter Randomized Controlled Clinical Trial of Indocyanine Green Molecular Fluorescence Imaging in the Diagnosis and Treatment of Primary Liver Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05160740
Acronym
ICGMFITinPLC
Enrollment
348
Registered
2021-12-16
Start date
2021-09-23
Completion date
2025-12-31
Last updated
2022-02-04

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

Conditions

Liver Cancer

Keywords

indocyanine green, local resection

Brief summary

The of this study is to explore the clinical outcomes of indocyanine green molecular fluorescence imaging in local resection of primary hepatocellular carcinoma (CNLC Ⅰa stage).

Detailed description

Indocyanine green molecular imaging technique is often used in the surgical treatment of primary liver cancer. Its application in hepatectomy of primary liver cancer is currently in the stage of case accumulation and clinical research. No prospective study has been conducted to determine the clinical efficacy of indocyanine green molecular imaging for local hepatectomy of primary liver cancer. On the basis of more than 1000 liver resection procedures, the investigators want to apply indocyanine green molecular imaging technology, a cheap, simple and radiation-free method, to guide surgical resection. The purpose is to assist surgical procedures and improve participants' tumor-free survival.

Interventions

ICG will be injected to participants preoperatively for molecular fluorescence image

Sponsors

Zhujiang Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 66 Years
Healthy volunteers
No

Inclusion criteria

* First clinical diagnosis of primary liver cancer (China liver cancer staging, CNLC Ia stage); * Child-Pugh grading standard of liver function was GRADE A or B; * 18-66 years old; * Complete clinical case data; * limited surgical methods (local resection); * Voluntarily participate in the study and sign the informed consent.

Exclusion criteria

* There are basic diseases that cannot tolerate surgery (such as severe cardiopulmonary cerebral renal insufficiency); * Tumor thrombus or distant metastasis was found in main portal vein and primary branch, main hepatic vein and branch, main hepatic vein and inferior vena cava by preoperative imaging examination; * planned pregnancy, unplanned pregnancy and pregnancy; * Preoperative child-Pugh grading standard of liver function was Grade C. * Disease researchers that the investigator considers inappropriate to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frameDescription
3-year disease free survival rate36 monthsNo tumor recurrence within 3 years after surgery divided by total number of patients

Secondary

MeasureTime frameDescription
Positive margin rate14 daysCompare positive margin rate in both groups
Length of the shortest cutting edge14 daysThe shortest distance between tumor and resection margin was compared between the two groups by pathological diagnosis
Operation time1 dayCompare operation time in both groups
Intraoperative blood loss1 dayCompare intraoperative blood loss in both groups
Intraoperative blood transfusion volume1 dayCompare intraoperative blood transfusion volume in both groups
The number of small lesions of HCC14 daysSmall lesions detected by ICG fluorescence and confirmed by pathology in the intervention group
Residual tumor at the margin of liver cross-section14 daysThe number of residual tumors confirmed by ICG fluorescence detection at the liver margin of the intervention group
Intraoperative biliary fistula detection rate1 dayThe number of cases of successful intraoperative detection of biliary fistula by fluorescence in the intervention group divided by the total number of cases in the intervention group.
Extrahepatic metastases of primary hepatocellular carcinoma14 daysThe number of extrahepatic metastases of primary liver cancer detected by ICG and confirmed by pathology in the intervention group
Negative margin rate14 daysCompare negative margin rate in both groups
Postoperative liver function index 15 daysCompare the levels of Alanine aminotransferase on postoperative days 1, 3, and 5 in both groups
Postoperative liver function index 25 daysCompare the levels of Aspartate aminotransferase on postoperative days 1, 3, and 5 in both groups
Postoperative liver function index 35 daysCompare the levels of serum albumin on postoperative days 1, 3, and 5 in both groups
Postoperative liver function index 45 daysCompare the levels of total bilirubin on postoperative days 1, 3, and 5 in both groups
Postoperative hemoglobin5 daysCompare hemoglobin on postoperative days 1, 3, and 5 in both groups
Postoperative platelets5 daysCompare platelets on postoperative days 1, 3, and 5 in both groups
Prothrombin time5 daysCompare prothrombin time on postoperative days 1, 3, and 5 in both groups
Mortality rates3 monthsPerioperative death was defined as death occurring within 90 days after surgery
Postoperative hospital stay30 daysCompare Postoperative hospital stay in both groups. Eg: Postoperative hospital stay is the number of days from the day of surgery to the day of discharge.

Countries

China

Contacts

Primary ContactChihua Fang, MD
fangchihua@smu.edu.cn13609700805
Backup ContactXiaojun Zeng
zengxiaojun95@126.com15626104890

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026