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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04759820
Other study ID # CRC-SH02
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date January 1, 2021
Est. completion date June 30, 2023

Study information

Verified date February 2021
Source Fudan University
Contact Xinxiang Li, MD
Phone 86-21-64175590
Email lxx1149@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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 tracer in colorectal cancer, in order to further improve postoperative lymph node inspection, precise postoperative adjuvant therapy and improve the patients' long-term survival.


Recruitment information / eligibility

Status Recruiting
Enrollment 298
Est. completion date June 30, 2023
Est. primary completion date June 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: 1. Colorectal cancer was confirmed by preoperative fibrocolonoscopy and pathological examination; 2. 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; 3. The lower edge of the lesion is located more than 10cm from the anus; 4. Age 18 ~ 70; 5. 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. 6. Patients had no psychological, family, social, or geographical constraints that affected protocol compliance and follow-up time 7. Patient signs informed consent; Exclusion Criteria: 1. Under 18 years old or above 70 years old; 2. Other types of colorectal cancer (adenosquamous cell carcinoma, squamous cell carcinoma, neuroendocrine tumor, clear cell carcinoma, spindle cell carcinoma, undifferentiated carcinoma) 3. Rectum cancer less than 10cm from the anus; 4. Previous abdominal surgery; 5. Neoadjuvant therapy was received preoperatively, including radiotherapy and chemotherapy; 6. Due to various reasons, preoperative colonoscopic injection of carbon nanoparticles/indocyanine green labeling was not possible; 7. Intraoperative radical surgery cannot be performed due to various reasons; 8. Acute abdomen: intestinal obstruction, intestinal wringing, peritonitis, etc.; 9. Combined with other site metastasis; 10. Have severe heart, lung, liver and kidney diseases and cannot tolerate surgery; 11. Active stage of liver disease or abnormal liver function, ALT, AST, TBIL more than twice the upper limit of normal value; 12. Renal function impairment, Cr=2 times the upper limit of normal or BUN=2 times the upper limit of normal; 13. 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; 14. People with mental illness or mental retardation who cannot describe their feelings correctly; 15. Severe disorder of coagulation mechanism and bleeding tendency; 16. Have a history of serious uncontrolled medical disease or recent myocardial infarction (within 3 months);Acute infection; 17. Patients with uncontrolled severe hypertension and severe diabetes after intervention treatment; 18. Allergic to the test drug; 19. A history of alcohol, drug or substance abuse; 20. Participants who had participated in any drug trial within 3 months prior to enrollment; 21. Other subjects considered by the researcher to be unsuitable for inclusion in this study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
injecting Carbon Nanoparticles Suspension
injecting Carbon Nanoparticles Suspension for lymph node detection
Injecting indocyanine green
Injecting indocyanine green for lymph node detection

Locations

Country Name City State
China Fudan University Shanghai Cancer Center Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
LI XIN-XIANG

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of lymph nodes detected 1 week after surgery
Primary Number of positive lymph nodes detected at different T stages 1 week after surgery
Primary the ratio of positive lymph nodes 1 week after surgery
Secondary patients' Disease-Free Survival(DFS) 1 year after surgery