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临床试验/NCT06793280
NCT06793280已完成不适用

Evaluation of Colonic Perfusion by Indocyanine Green Angiography During Elective Colorectal Surgery: Randomized Controlled Trial

University of Roma La Sapienza1 个研究点 分布在 1 个国家目标入组 562 人开始时间: 2022年2月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
562
试验地点
1
主要终点
Anastomotic leak rate

研究概览

简要总结

Despite advancements in technology and improved surgical techniques, the occurrence of anastomotic leakage (AL) after colorectal surgery remains between 4% and 30%. AL is a feared complication associated with significant morbidity and mortality in colorectal surgery, with its causes being multifaceted. Inadequate blood supply to the intestines is believed to be a major contributor to its development. Various methods have been proposed to objectively assess intestinal perfusion beyond the subjective evaluation done by surgeons during surgery. However, these methods face challenges such as poor reproducibility and high costs, limiting their routine use. In recent years, indocyanine green (ICG) angiography has emerged as a tool for assessing organ perfusion in various medical scenarios. However, only one randomized clinical trial has been conducted regarding its use in evaluating colorectal surgery outcomes, which found that while ICG angiography sometimes led to additional bowel resection, it didn't significantly reduce the rate of anastomotic leaks compared to conventional methods. This could be due to the trial's small sample size, potentially reducing its statistical power. This study aims to investigate whether ICG angiography can lower the rate of anastomotic leaks during laparoscopic colorectal cancer surgery, while also examining its impact on resection margins, perioperative morbidity, and mortality rates.

A total of 561 subjects undergoing laparoscopic colorectal surgery for malignancy, will be randomized in 2 arms: A Study Group undergoing ICG angiography (i.e. colonic perfusion is intraoperatively assessed by ICG angiography and level of resection is selected based on the fluorescence) and a Control Group (i.e. resection is performed based on subjective judgment).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age: 18-85 years
  • •Malignant colorectal tumors
  • •Elective surgery

排除标准

  • •Abdomino-perineal resection
  • •Emergency procedures
  • •Conversion to open surgery
  • •No anastomosis
  • •Multifocal tumors
  • •Locally advanced cancer (T4)
  • •Distant metastases (M+)
  • •Major vasculopathies (previous PE, DVT, abdominal aorta surgery)
  • •ICG allergy

研究组 & 干预措施

No ICG angiography

Active Comparator

Subjective visual measures are employed by the surgeon in order to determine anastomotic perfusion.

干预措施: No intraoperative ICG angiography (Procedure)

ICG angiography

Experimental

luorescence angiography is utilized to assess colonic resection margins and colorectal anastomosis, aiming to evaluate colonic blood flow. If the assessment indicates "insufficient" perfusion at the resection margin, the colon is resected once more to ensure satisfactory blood flow.

luorescence angiography is utilized to assess colonic resection margins and colorectal anastomosis, aiming to evaluate colonic blood flow. If the assessment indicates "insufficient" perfusion at the resection margin, the colon is resected once more to ensure satisfactory blood flow.

Colonic resection margins and colorectal anastomosis are intraoperatively assessed using fluorescence angiography to evaluate colonic perfusion. If perfusion at resection margin is considered "insufficient" the colon is resected again in order to obtain adequate perfusion.

干预措施: intraoperative ICG angiography (Procedure)

结局指标

主要结局

Anastomotic leak rate

时间窗: 90 days

次要结局

  • Hospital re-admissions(30 days)
  • Modification in the level of resection margins (cm)(intraoperative)
  • RCP levels (POD 3, 5)(5 days)
  • Early complications (30 days)(30 days)
  • Mortality(90 days)
  • Operative time(1 day)

研究者

发起方
University of Roma La Sapienza
申办方类型
Other
责任方
Principal Investigator
主要研究者

Lidia Castagneto Gissey

Professor

University of Roma La Sapienza

研究点 (1)

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