Liver Cancer Clinical Trial
— ICGMFITinPLCOfficial title:
Multicenter Randomized Controlled Clinical Trial of Indocyanine Green Molecular Fluorescence Imaging in the Diagnosis and Treatment of Primary Liver Cancer
The of this study is to explore the clinical outcomes of indocyanine green molecular fluorescence imaging in local resection of primary hepatocellular carcinoma (CNLC â… a stage).
Status | Recruiting |
Enrollment | 348 |
Est. completion date | December 31, 2025 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 66 Years |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
China | Zhujiang Hospital of Southern Medical University | Guangzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Zhujiang Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 3-year disease free survival rate | No tumor recurrence within 3 years after surgery divided by total number of patients | 36 months | |
Secondary | Positive margin rate | Compare positive margin rate in both groups | 14 days | |
Secondary | Negative margin rate | Compare negative margin rate in both groups | 14 days | |
Secondary | Length of the shortest cutting edge | The shortest distance between tumor and resection margin was compared between the two groups by pathological diagnosis | 14 days | |
Secondary | Operation time | Compare operation time in both groups | 1 day | |
Secondary | Intraoperative blood loss | Compare intraoperative blood loss in both groups | 1 day | |
Secondary | Intraoperative blood transfusion volume | Compare intraoperative blood transfusion volume in both groups | 1 day | |
Secondary | The number of small lesions of HCC | Small lesions detected by ICG fluorescence and confirmed by pathology in the intervention group | 14 days | |
Secondary | Residual tumor at the margin of liver cross-section | The number of residual tumors confirmed by ICG fluorescence detection at the liver margin of the intervention group | 14 days | |
Secondary | Intraoperative biliary fistula detection rate | 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. | 1 day | |
Secondary | Extrahepatic metastases of primary hepatocellular carcinoma | The number of extrahepatic metastases of primary liver cancer detected by ICG and confirmed by pathology in the intervention group | 14 days | |
Secondary | Postoperative hospital stay | 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. | 30 days | |
Secondary | Postoperative liver function index 1 | Compare the levels of Alanine aminotransferase on postoperative days 1, 3, and 5 in both groups | 5 days | |
Secondary | Postoperative liver function index 2 | Compare the levels of Aspartate aminotransferase on postoperative days 1, 3, and 5 in both groups | 5 days | |
Secondary | Postoperative liver function index 3 | Compare the levels of serum albumin on postoperative days 1, 3, and 5 in both groups | 5 days | |
Secondary | Postoperative liver function index 4 | Compare the levels of total bilirubin on postoperative days 1, 3, and 5 in both groups | 5 days | |
Secondary | Postoperative hemoglobin | Compare hemoglobin on postoperative days 1, 3, and 5 in both groups | 5 days | |
Secondary | Postoperative platelets | Compare platelets on postoperative days 1, 3, and 5 in both groups | 5 days | |
Secondary | Prothrombin time | Compare prothrombin time on postoperative days 1, 3, and 5 in both groups | 5 days | |
Secondary | Mortality rates | Perioperative death was defined as death occurring within 90 days after surgery | 3 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03213314 -
HepaT1ca: Quantifying Liver Health in Surgical Candidates for Liver Malignancies
|
N/A | |
Not yet recruiting |
NCT04931420 -
Study Comparing Standard of Care Chemotherapy With/ Without Sequential Cytoreductive Surgery for Patients With Metastatic Foregut Cancer and Undetectable Circulating Tumor-Deoxyribose Nucleic Acid Levels
|
Phase 2 | |
Terminated |
NCT00788125 -
Dasatinib, Ifosfamide, Carboplatin, and Etoposide in Treating Young Patients With Metastatic or Recurrent Malignant Solid Tumors
|
Phase 1/Phase 2 | |
Completed |
NCT03756597 -
PAN-study: Pan-Cancer Early Detection Study (PAN)
|
||
Completed |
NCT01906021 -
Study of New Software Used During Ablations
|
N/A | |
Terminated |
NCT04589884 -
Intraoperative EXamination Using MAChine-learning-based HYperspectral for diagNosis & Autonomous Anatomy Assessment
|
||
Recruiting |
NCT05953337 -
Radioembolization Trial Utilizing Eye90 Microspheres™ for the Treatment of Hepatocellular Carcinoma (HCC)
|
N/A | |
Enrolling by invitation |
NCT04466124 -
Prospective Cohort Study of Liver Cancer Patients Treated With Proton Beam Therapy
|
||
Not yet recruiting |
NCT04053231 -
Hepatocarcinoma Recurrence on the Liver Study - Part2
|
||
Active, not recruiting |
NCT02869217 -
Study of TBI-1301 (NY-ESO-1 Specific TCR Gene Transduced Autologous T Lymphocytes) in Patients With Solid Tumors
|
Phase 1 | |
Completed |
NCT03059238 -
Parecoxib Versus Celecoxib Versus Oxycodone in Pain Control for Transcatheter Chemoembolization Procedure
|
Phase 3 | |
Recruiting |
NCT02632188 -
Radical Surgery Followed by Immunotherapy Using Precision T Cells Specific to Multiple Common Tumor-Associated Antigen for the Treatment of Hepatocellular Carcinoma
|
Phase 1/Phase 2 | |
Recruiting |
NCT01388101 -
Real-time Diagnosis of Serum LECT 2 in Patient With Liver Cancer Using Electronic Antibody Sensor (e- Ab Sensor)
|
N/A | |
Completed |
NCT01042041 -
Sorafenib Tosylate and Chemoembolization in Treating Patients With Unresectable Liver Cancer
|
Phase 1 | |
Completed |
NCT00980239 -
HAI Irinotecan + IV Bevacizumab, Bevacizumab & Oxaliplatin or Bevacizumab & Cetuximab in Advanced Cancers Metastatic to Liver
|
Phase 1 | |
Terminated |
NCT00903396 -
Palonosetron Hydrochloride in Preventing Nausea and Vomiting Caused by Radiation Therapy in Patients With Primary Abdominal Cancer
|
Phase 2 | |
Completed |
NCT00790569 -
Varenicline or Nicotine Patch and Nicotine Gum in Helping Smokers in a Methadone Treatment Program Stop Smoking
|
N/A | |
Completed |
NCT00543777 -
Magnetic Resonance Elastography and 2-Point Dixon MR Imaging Techniques in Diffuse Liver Disease
|
Phase 1/Phase 2 | |
Terminated |
NCT00896467 -
Psychological and Emotional Impact in Patients Undergoing Treatment For Metastatic Cancer Either in a Clinical Trial or as Standard Off-Trial Therapy
|
N/A | |
Completed |
NCT00888407 -
Community-based Hepatitis B Interventions for Hmong Adults
|
N/A |