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临床试验/NCT01146743
NCT01146743已完成不适用

Prospective Randomized Controlled Trial for Endoscopic Ultrasound Guided and Percutaneous Transhepatic Gallbladder Drainage for Acute Cholecystitis in High Risk Patients

Asan Medical Center1 个研究点 分布在 1 个国家目标入组 59 人开始时间: 2010年6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
已完成
入组人数
59
试验地点
1
主要终点
Clinical response rate

研究概览

简要总结

The investigators would like to conduct a prospective, randomized non-inferiority study to compare clinical outcome between endoscopic ultrasound (EUS) guided gallbladder drainage and percutaneous transhepatic gallbladder drainage (PTGBD) in high risk acute cholecystitis patients.

详细描述

The primary outcome is to compare clinical resolution rate of EUS-guided gallbladder drainage versus percutaneous transhepatic gallbladder drainage in acute cholecystitis patients with high risk.

The secondary outcome is to compare complications, conversion rate to open cholecystectomy during laparoscopic cholecystectomy.

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
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
否

入选标准

  • •high risk for general anesthesia and emergency operation (American Society of Anesthesiologists, ASA grade III or IV)

排除标准

  • •Age below 18 years
  • •Pregnancy
  • •When the risks of endoscopy to patient are judged to outweigh the most favorable benefits of the procedure.
  • •Unstable or unwilling to comply with follow-up
  • •When a perforated viscus is known or suspected
  • •Simultaneously participating in another investigational drug or device study

研究组 & 干预措施

EUS-guided

Active Comparator

EUS-guided gallbladder drainage in acute cholecystitis with high risk patients

干预措施: EUS-guided gallbladder drainage (Procedure)

percutaneous transhepatic

Active Comparator

percutaneous transhepatic gallbladder drainage in acute cholecystitis with high risk patients

干预措施: percutaneous transhepatic gallbladder drainage (Procedure)

结局指标

主要结局

Clinical response rate

时间窗: Within 72 hours from procedure

Definition of clinical response rate within 72 hours from procedure was improvement of local signs and systemic signs of inflammation.

次要结局

  • Complication rate(Complications during the procedure or within 1 weeks)
  • Conversion rate(During laparoscopic cholectstectomy)

研究者

申办方类型
Other

研究点 (1)

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