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

Sponsor
Zhujiang Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05160740
Collaborator
(none)
348
1
2
51.3
6.8

Study Details

Study Description

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).

Condition or Disease Intervention/Treatment Phase
  • Drug: Indocyanine green for injection
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
348 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Multicenter Randomized Controlled Clinical Trial of Indocyanine Green Molecular Fluorescence Imaging in the Diagnosis and Treatment of Primary Liver Cancer
Actual Study Start Date :
Sep 23, 2021
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: ICG molecular fluorescence imaging guided surgery

ICG molecular fluorescence imaging will be used in local hepatectomy of primary liver cancer in this group

Drug: Indocyanine green for injection
ICG will be injected to participants preoperatively for molecular fluorescence image
Other Names:
  • ICG
  • Placebo Comparator: No ICG molecular fluorescence imaging guided surgery

    ICG molecular fluorescence imaging will not be used in local hepatectomy of primary liver cancer in this group

    Drug: Indocyanine green for injection
    ICG will be injected to participants preoperatively for molecular fluorescence image
    Other Names:
  • ICG
  • Outcome Measures

    Primary Outcome Measures

    1. 3-year disease free survival rate [36 months]

      No tumor recurrence within 3 years after surgery divided by total number of patients

    Secondary Outcome Measures

    1. Positive margin rate [14 days]

      Compare positive margin rate in both groups

    2. Negative margin rate [14 days]

      Compare negative margin rate in both groups

    3. Length of the shortest cutting edge [14 days]

      The shortest distance between tumor and resection margin was compared between the two groups by pathological diagnosis

    4. Operation time [1 day]

      Compare operation time in both groups

    5. Intraoperative blood loss [1 day]

      Compare intraoperative blood loss in both groups

    6. Intraoperative blood transfusion volume [1 day]

      Compare intraoperative blood transfusion volume in both groups

    7. The number of small lesions of HCC [14 days]

      Small lesions detected by ICG fluorescence and confirmed by pathology in the intervention group

    8. Residual tumor at the margin of liver cross-section [14 days]

      The number of residual tumors confirmed by ICG fluorescence detection at the liver margin of the intervention group

    9. Intraoperative biliary fistula detection rate [1 day]

      The 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.

    10. Extrahepatic metastases of primary hepatocellular carcinoma [14 days]

      The number of extrahepatic metastases of primary liver cancer detected by ICG and confirmed by pathology in the intervention group

    11. Postoperative hospital stay [30 days]

      Compare 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.

    12. Postoperative liver function index 1 [5 days]

      Compare the levels of Alanine aminotransferase on postoperative days 1, 3, and 5 in both groups

    13. Postoperative liver function index 2 [5 days]

      Compare the levels of Aspartate aminotransferase on postoperative days 1, 3, and 5 in both groups

    14. Postoperative liver function index 3 [5 days]

      Compare the levels of serum albumin on postoperative days 1, 3, and 5 in both groups

    15. Postoperative liver function index 4 [5 days]

      Compare the levels of total bilirubin on postoperative days 1, 3, and 5 in both groups

    16. Postoperative hemoglobin [5 days]

      Compare hemoglobin on postoperative days 1, 3, and 5 in both groups

    17. Postoperative platelets [5 days]

      Compare platelets on postoperative days 1, 3, and 5 in both groups

    18. Prothrombin time [5 days]

      Compare prothrombin time on postoperative days 1, 3, and 5 in both groups

    19. Mortality rates [3 months]

      Perioperative death was defined as death occurring within 90 days after surgery

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 66 Years
    Sexes Eligible for Study:
    All
    Accepts 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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Zhujiang Hospital of Southern Medical University Guangzhou Guangdong China 510282

    Sponsors and Collaborators

    • Zhujiang Hospital

    Investigators

    • Study Chair: Chihua Fang, MD, Zhujiang Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Chihua Fang,MD, Clinical Professor, Zhujiang Hospital
    ClinicalTrials.gov Identifier:
    NCT05160740
    Other Study ID Numbers:
    • 2021-KY-090-01
    First Posted:
    Dec 16, 2021
    Last Update Posted:
    Feb 4, 2022
    Last Verified:
    Jan 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Chihua Fang,MD, Clinical Professor, Zhujiang Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 4, 2022