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临床试验/NCT06918210
NCT06918210尚未招募不适用

Indocyanine Green Fluorescence During Fundus First Laparoscopic Cholecystectomy

Karolinska Institutet0 个研究点目标入组 294 人开始时间: 2025年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
294
主要终点
Time to intraoperative cholangiography

研究概览

简要总结

Laparoscopic cholecystectomy is the routine method for managing gallstone disease. This is considered a safe procedure with low risk of severe complications. Lesions to the deep bile ducts is, however, a rare complication from laparoscopic cholecystectomy that may have devastating consequences. The risk of bile duct injuries may be reduced by adapting the surgical approach. In general, the operation is started from the lower part of the gallbladder and continued upwards. It may, however, also be initiated from the top of the gallbladder and extended downwards. This approach, also termed fundus first, is routine at a few units.

By injecting Indocyanin Green (ICG) that is excreted into the bile, the bile ducts may be visualized using near infrared light. This is a technique for mapping the anatomical structures adjacent to the gallbladder that has been used in previous studies for preventing bile duct injuries. This method has, however, not been tested at units where fundus first is the routine surgical technique. In the present randomized controlled trial, the investigators intend to evaluate the safety of ICG as a means for reducing the risk of bile duct lesions and to see if it works as intended.

Altogether 294 operations for gallstones will be included in the study. The patients will be randomized to surgery with or without ICG. Regardless of the randomization, all operations will be undertaken with the fundus first technique.

Thirty days after the operation, all data related to the operation are retrieved from the patient records by an assessor that does not know what group the patient was randomized to. The primary endpoint of the study is the time required from the start of the operation until intraoperative cholangiography is done. In addition, total operative time, all surgical complications and need for converting the operation to an open procedure will be recorded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • •Patients undergoing laparoscopic cholecystectomy
  • •Verbal and written consent provided
  • •Age ≥ 18 years

排除标准

  • •Thyroid disease
  • •Allergy against ICG or Iodine

研究组 & 干预措施

Visualization with ICG

Experimental

Intraoperative visualization of the bile ducts with ICG and near infrared light

干预措施: Cholangiography (Procedure)

Comparator

Active Comparator

Visualization of the bile ducts with intraoperative cholangiography only.

干预措施: Cholangiography (Procedure)

Visualization with ICG

Experimental

Intraoperative visualization of the bile ducts with ICG and near infrared light

干预措施: Indocyanine Green (Procedure)

结局指标

主要结局

Time to intraoperative cholangiography

时间窗: During procedure.

Time from first incision until intraoperative cholangiography

次要结局

  • Procedure-related complications(Up to 30 days postoperatively)
  • Total operative time(During procedure)
  • Intraoperative gallbladder perforation(During procedure)
  • Conversion from laparoscopic to open cholecystectomy(During procedure)
  • Surgeon perception of complexity(During procedure)
  • Patient reported outcome(Up to 30 days postoperatively)

研究者

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

Gabriel Sandblom

Associate Professor

Karolinska Institutet

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