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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04207489
Other study ID # 130003
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 15, 2020
Est. completion date April 28, 2021

Study information

Verified date August 2020
Source Jilin University
Contact Hong Xu, Professor
Phone 18243052038
Email yd18243052038@163.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Prospective registry study of endoscopic submucosal injection of indocyanine green before laparoscopic radical resection for colorectal cancer


Description:

To observe the imaging result of endoscopic submucosal injection of indocyanine green before laparoscopic radical resection for colorectal cancer, and analyze the relevant factors, so as to guide the submucosal injection of preoperative indocyanine green better.

This study is prospective and observational. In order to analyze the related factors that affect the imaging effect, we enrolled patients who were to undergo indocyanine green fluorescence imaging for laparoscopic radical resection for colorectal cancer.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date April 28, 2021
Est. primary completion date December 25, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients who were to undergo indocyanine green fluorescence imaging for laparoscopic radical operation of colorectal cancer.

Exclusion Criteria:

- have simultaneously other cancer

- have severe systemic inflammatory disease ,serious illness such as diabetes, chronic lung diseases

- have gastrointestinal surgery

- Indocyanine green or iodine allergy

- the period is too late or the tumor is too large to carry on a laparoscopic surgery.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
endoscopic submucosal injection of indocyanine green before laparoscopic radical operation of colorectal cancer
Indocyanine green was injected under endoscope within 24 hours before operation. Four points were evenlyinjected in four quadrants at the edge of the tumor. The patients with obstruction were injected at two points on the anal side of the tumor. The diluted concentration of indocyanine green was 0.625mg/ml or 1.25mg/ml. The injection method was direct submucosal injection and sandwich method. According to the imaging effect, it can be divided into local imaging and lymphatic drainage imaging. Tumor body: 0, no imaging; 1, full imaging; 2, diffuse imaging, overflow, interference with other areas of observation. Lymph drainage area imaging 0, no imaging; 1, full imaging; 2, diffuse imaging, overflow, interference with other areas of observation.

Locations

Country Name City State
China the First Hospital of Jilin University Chang chun Ji Lin

Sponsors (1)

Lead Sponsor Collaborator
Jilin University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The imaging effect of indocyanine green The imaging effect was evaluated by indocyanine green fluorescence imaging system during the operation. According to the imaging effect, it can be divided into local imaging and lymphatic drainage imaging. Tumor body: 0, no imaging; 1, full imaging; 2, diffuse imaging, overflow, interference with other areas of observation. Lymph drainage area imaging 0, no imaging; 1, full imaging; 2, diffuse imaging, overflow, interference with other areas of observation. During the operation
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