Status:
UNKNOWN
Carbon Nanoparticles vs Indocyanine Green
Lead Sponsor:
LI XIN-XIANG
Conditions:
Number of Lymph Node Retrieved
Eligibility:
All Genders
18-70 years
Phase:
PHASE2
PHASE3
Brief Summary
Both nano carbon and ICG as lymph node tracers in colorectal cancer have their own value, this study was to contrast two tracers in colorectal cancer surgeries, so as to find out the best lymphnode tr...
Eligibility Criteria
Inclusion
- Colorectal cancer was confirmed by preoperative fibrocolonoscopy and pathological examination;
- The operative requirements of the patients included in the study: laparoscopic radical surgery of colon/rectal cancer, indocyanine green group should be used fluorescent laparoscopic (Pinpoint) surgery;
- The lower edge of the lesion is located more than 10cm from the anus;
- Age 18 \~ 70;
- The results of laboratory examination before enrollment met the following surgical conditions: neutrophils (ANC) ≥1.5×109/L, platelets (PLT) ≥ 100×109/L, total bilirubin (TBI) ≤1.5× upper limit of normal (2mg/ dL), alanine aminotransferase (ALT), ascarate aminotransferase (AST) ≤2× upper limit of normal;The coagulation parameters were in the normal range.
- Patients had no psychological, family, social, or geographical constraints that affected protocol compliance and follow-up time
- Patient signs informed consent;
Exclusion
- Under 18 years old or above 70 years old;
- Other types of colorectal cancer (adenosquamous cell carcinoma, squamous cell carcinoma, neuroendocrine tumor, clear cell carcinoma, spindle cell carcinoma, undifferentiated carcinoma)
- Rectum cancer less than 10cm from the anus;
- Previous abdominal surgery;
- Neoadjuvant therapy was received preoperatively, including radiotherapy and chemotherapy;
- Due to various reasons, preoperative colonoscopic injection of carbon nanoparticles/indocyanine green labeling was not possible;
- Intraoperative radical surgery cannot be performed due to various reasons;
- Acute abdomen: intestinal obstruction, intestinal wringing, peritonitis, etc.;
- Combined with other site metastasis;
- Have severe heart, lung, liver and kidney diseases and cannot tolerate surgery;
- Active stage of liver disease or abnormal liver function, ALT, AST, TBIL more than twice the upper limit of normal value;
- Renal function impairment, Cr≥2 times the upper limit of normal or BUN≥2 times the upper limit of normal;
- The subjects' white blood cells are lower than the lower limit of normal value, or their platelets are lower than the lower limit of normal value, or have other diseases of the blood system;
- People with mental illness or mental retardation who cannot describe their feelings correctly;
- Severe disorder of coagulation mechanism and bleeding tendency;
- Have a history of serious uncontrolled medical disease or recent myocardial infarction (within 3 months);Acute infection;
- Patients with uncontrolled severe hypertension and severe diabetes after intervention treatment;
- Allergic to the test drug;
- A history of alcohol, drug or substance abuse;
- Participants who had participated in any drug trial within 3 months prior to enrollment;
- Other subjects considered by the researcher to be unsuitable for inclusion in this study.
Key Trial Info
Start Date :
January 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 30 2023
Estimated Enrollment :
298 Patients enrolled
Trial Details
Trial ID
NCT04759820
Start Date
January 1 2021
End Date
June 30 2023
Last Update
February 18 2021
Active Locations (1)
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1
Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality, China, 200032