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临床试验/NCT05153954
NCT05153954已完成不适用

Quantitative ICG Fluorescence Angiography in Colorectal Surgery (QUANTICO): a Protocol for a Prospective, Standardized, Observational, Surgeon-blinded Multi-center Trial

Zealand University Hospital2 个研究点 分布在 1 个国家目标入组 114 人开始时间: 2021年8月31日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
114
试验地点
2
主要终点
Postoperative anastomotic complications

研究概览

简要总结

Fluorescence angiography with indocyanine green (ICG-FA) has gained increased popularity in colorectal surgery to check perfusion to the newly-formed anastomotic area and decrease the rate of postoperative anastomotic leakage.

While qualitative ICG assessment has the advantage to be used instantly during the operative procedure, it does bear drawbacks (subjective assessment, dependent on factors like camera distance, ICG dose and white-light contamination).

The alternative is quantitative ICG assessment, which is performed by evaluating the time-intensity curve of the ICG-FA with an external analyzing software. The procedure is showing promising results, but the methodology is still reported very heterogeneously.

This study is a multi-center, prospective, standardized, surgeon-blinded observational trial. The key aspect of this study is the non-interventional design with blinding of both the qualitative and quantitative results from the ICG perfusion measurement, providing no chance of influencing the course of the operation. Assessment of perfusion will be performed postoperatively blinded to the outcome. Assessment of the pre-anastomotic area is intraoperatively performed by an image analysis software that then calculates a perfusion score based on an algorithm integrating relevant perfusion metrics. The primary outcome is the combined rate of early and late anastomotic complications within 90 days postoperatively.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Age 18 years or older
  • Capable of giving informed consent
  • ASA Classification: status I-III
  • Planned for PME or TME with minimally invasive approach and primary anastomosis
  • Strong suspicion of or biopsy-verified sigmoid or rectal cancer Stage I-IV cancer

排除标准

  • Known allergy to ICG or iodine
  • Emergency procedure
  • Pregnancy or if the patient is currently nursing
  • Surgeons decide to do unblinded quantitative or qualitative ICG-FA

结局指标

主要结局

Postoperative anastomotic complications

时间窗: 3 months

combined rate of all anastomotic complications

次要结局

  • Duration of surgery(1 day)
  • Hospital readmission(1 month)
  • Number of participants with anastomotic leakage rate, severity (grade A-C)(90 days)
  • Number of participants with wound dehiscence(1 month)
  • Number of participants with postoperative bleeding(10 days)
  • Comprehensive complications index(90 days)
  • Reoperation rate(1 month)
  • QT interval variability(2 days)
  • Number of participants with complications according to Clavien-Dindo Classification(90 days)
  • Number of participants with postoperative paralytic ileus(90 days)
  • Length of hospital stay(1 month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Carolin Oppermann

Medical Doctor, PhD student

Zealand University Hospital

研究点 (2)

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