跳至主要内容
临床试验/NCT05041686
NCT05041686已完成不适用

A Prospective, Multi-site, Single Cohort, Non-controlled, Non-randomized Clinical Trial Evaluating the Usefulness of CADISS® System for the Cleavage of Severe Adhesions in Acute Cholecystitis (Cholecystectomy)

AuXin Surgery SA2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2019年5月30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
15
试验地点
2
主要终点
Ability of the CADISS® System to dissect adherences without cutting

研究概览

简要总结

Acute cholecystitis is the most common complication of cholelithiasis. Acute cholecystitis is inflammation of the gallbladder that develops over hours, usually due to an obstruction of the cystic duct by a gallstone. Removal of the gallbladder (Cholecystectomy) is the only definitive treatment for acute cholecystitis, with laparoscopic cholecystectomy (LC) considered the gold standard. Serious complications that may occur with laparoscopic cholecystectomy, including bile duct injury, bile leaks, bleeding, and bowel injury, result in part from the anatomy, disease related pathology and structural misidentification due to inflammatory process (Gupta 2019).

The CADISS® System, Chemically Assisted mechanical DISSection, is intended for the selective detachment of pathological tissue layers and/or fibrotic tissues in various surgical procedures without using cutting instruments. It is based on the property of the drug mesna (Sodium 2-mercaptoethane sulfonate) to cleave the disulfide bonds responsible for the adherence of pathological tissues and for the strength of fibrosis. This study is a prospective, multi-sites, open label, single cohort clinical trial evaluating the use of CADISS® system to facilitate dissection of severe adhesions in cholecystectomy and to allow better identification of different structure.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

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

  • ≥ 18 years old
  • Weight > 30 kg
  • Confirmed diagnosis of acute gallstone cholecystitis
  • Symptomatic or asymptomatic cholecystitis
  • Under surgery for cholecystectomy:
  • for the 5 first patients : cholecystectomy will take place within 72 hours of the first symptoms of cholecystitis
  • after the 5 first patients : cholecystectomy will be allowed at any time after the first symptoms and at physician judgment
  • Patient agrees to signed the informed consent

排除标准

  • < 18 years old
  • Known hypersensibility to mesna
  • Patient taking anticoagulant at the screening visit
  • Patient having a pancreatitis or angiocholitis
  • Patients suffering from hepatic or renal disorders
  • Unable to sign the informed consent
  • Participation in any study involving an investigational drug or device within the past 3 Months.
  • Patient is pregnant, breastfeeding or has wish of pregnancy during the study.
  • Individuals under tutorship or trusteeship

结局指标

主要结局

Ability of the CADISS® System to dissect adherences without cutting

时间窗: Surgery

Percentage of successful dissection

次要结局

  • Adverse events(Surgery, 2 to 5 days after surgery (Hospital discharge), 6 weeks follow-up)
  • The change of bleeding with the use of the CADISS System(Surgery)
  • A change of surgical complication risk(Surgery)
  • The capability of the CADISS System to highlight the cleavage plane(Surgery)
  • The facilitation of detachment with the CADISS System(Surgery)
  • The ease of use of the CADISS System(Surgery)
  • The easiness of control of the topical application with the CADISS System(Surgery)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验