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临床试验/NCT01142921
NCT01142921终止不适用

A Prospective Randomised Study on the Patency Period of the Plastic Anti-reflux Biliary Stent

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2008年11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
终止
入组人数
16
试验地点
1
主要终点
time-to-occlusion or stent patency period in days

研究概览

简要总结

The aim of this study is to determine the average patency period of the new anti-reflux biliary stent on patients with malignant bile duct strictures and to determine if this stent remains patent for a longer period of time comparing with the ordinary plastic Tannenbaum biliary stent.

详细描述

Bile duct related cancer is a condition quite commonly seen among Asians. Predisposing conditions for primary bile duct cancer include recurrent infections and autoimmune diseases such as recurrent pyogenic cholangitis (RPC) and primary sclerosing cholangitis (PSC) as well as congenital problem such as choledochal cyst. Peri-ampullary tumour, pancreatic tumour and metastatic tumours with bile duct compression are other causes of bile duct obstruction. As many of these tumours are discovered at a late stage, curative treatment is usually not feasible. Palliative endoscopic stenting of the obstructed biliary system remains the treatment of choice for the majority.

The main problem with endoscopic stenting of the biliary system is the short stent patency period. There are some reports on modifications to plastic biliary stenting method in recent years including changes in stent designs, use of a different material or coating, administrating prophylactic antibiotics and the use of special drugs. All these have failed to show any conclusive effect on the stent patency period.

A preliminary study has demonstrated some promising results in the use of a stent with an anti-reflux property very similar to the stents the investigators are using in this study.

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age 18 years old
  • •Patients who have cholangiographic evidence (on ERCP) consistent with a malignant extrahepatic biliary stricture (below bifurcation of the common hepatic duct) who require plastic stenting
  • •Patients with peri-ampullary tumours, pancreatic tumours, gall bladder cancer and metastatic tumours with suspected extrinsic bile duct compression
  • •Patients with stent or nasobiliary drain in-situ without previous sphincterotomy will qualify for the study if they satisfy the above inclusion criteria.

排除标准

  • •Patients fit for surgery.
  • •Patients who have dominant biliary strictures involving the hilum or more proximal biliary segments.
  • •Previous sphincterotomy.
  • •Other medical conditions that will result in a life expectancy of less then 3 months (ASA class >4)
  • •Pregnancy

研究组 & 干预措施

Ordinary Tannenbaum biliary stent

Active Comparator

Ordinary Tannenbaum biliary stent

干预措施: Ordinary Tannenbaum biliary stent (Device)

Anti-reflux Tannenbaum biliary stent

Experimental

Anti-reflux Tannenbaum biliary stent

干预措施: Anti-reflux Tannenbaum biliary stent (Device)

结局指标

主要结局

time-to-occlusion or stent patency period in days

时间窗: within 25 weeks of device application

次要结局

  • Bleeding associated with endoscopic retrograde cholangiopancreatography (ERCP) and stent placement(within 25 weeks of device application)
  • perforation associated with ERCP and stent placement(within 25 weeks of device application)
  • pancreatitis associated with ERCP and stent placement(within 25 weeks of device application)
  • cholangitis associated with ERCP and stent placement(within 25 weeks of device application)
  • stent migration associated with ERCP and stent placement(within 25 weeks of device application)
  • all cause mortality(within 25 weeks of device application)

研究者

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

James Yun-wong Lau

Professor

Chinese University of Hong Kong

研究点 (1)

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