Carbon Nanoparticles vs Indocyanine Green

NCT ID: NCT04759820

Last Updated: 2021-02-18

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 298 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-01-01
• Study Completion Date: 2023-06-30

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

Conditions

Number of Lymph Node Retrieved

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Nano carbon group

Injection of carbon nanoparticle

Group Type: EXPERIMENTAL

injecting Carbon Nanoparticles Suspension

Intervention Type: DRUG

injecting Carbon Nanoparticles Suspension for lymph node detection

Indocyanine green group

Injection of indocyanine green

Group Type: ACTIVE_COMPARATOR

Injecting indocyanine green

Intervention Type: DRUG

Injecting indocyanine green for lymph node detection

Interventions

injecting Carbon Nanoparticles Suspension

injecting Carbon Nanoparticles Suspension for lymph node detection

Intervention Type: DRUG

Injecting indocyanine green

Injecting indocyanine green for lymph node detection

Intervention Type: DRUG

Eligibility Criteria

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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

LI XIN-XIANG

OTHER

Sponsor Role: lead

Responsible Party

LI XIN-XIANG

Professor

Responsibility Role: SPONSOR_INVESTIGATOR

Locations

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Xinxiang Li, MD

Role: CONTACT

lxx1149@163.com

86-21-64175590

Facility Contacts

Xinxiang Li, MD

Role: primary

lxx1149@163.com

86-21-64175590

Other Identifiers

CRC-SH02

Identifier Type: -

Identifier Source: org_study_id