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临床试验/NCT07115420
NCT07115420尚未招募不适用

Optimising EUS-guided Choledochoduodenostomy With Lumen Apposing Metal Stent With Stent in Stent Placement: a Randomised Study Between Double Pigtail Stent and Fully Covered Self-Expanding Metal Stent. The Opti-LAMS Study

Waikato Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年9月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
100
试验地点
1
主要终点
To compare the incidence of stent dysfunction (defined as recurrent jaundice and/or cholangitis) in patients with malignant biliary obstruction receiving FCSEMS vs DPS stent-in-stent through LAMS

研究概览

简要总结

This study looks at the best way to treat bile duct blockage in people with advanced cancer that cannot be removed by surgery. A blocked bile duct can cause serious symptoms like yellowing of the skin (jaundice), infection, and pain.

A common procedure called ERCP sometimes doesn't work in these patients. A newer method called EUS-guided choledochoduodenostomy (EUS-CDS) uses internal ultrasound to place a special metal tube (called a LAMS) to allow bile to drain. However, over time this stent can still become blocked.

To reduce this risk, doctors can place a second stent inside the first. This study is comparing two types of these second stents:

  • A plastic stent (double pigtail stent or DPS)
  • A metal stent (fully covered self-expanding metal stent or FCSEMS)

The study will include patients at Waikato Hospital. After the first stent is placed, they will be randomly assigned to receive either a DPS or FCSEMS. Patients will be followed for 6 months to see how well the stents work.

The aim is to find out which approach keeps the bile duct open longer and reduces the need for further procedures or hospitalisation, helping improve care and comfort for people with advanced cancer

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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

入选标准

  • Age ≥18 years.
  • Radiologically or histologically proven malignant distal bile duct obstruction with unresectable or metastatic disease, including those who have already failed ERCP
  • Indication for biliary drainage with presence of obstructive jaundice biochemically and dilated biliary system on imaging.
  • Informed consent provided.
  • Common bile duct (CBD) size of at least 12mm on EUS imaging

排除标准

  • Previous biliary stenting or surgery precluding EUS-CDS.
  • Inability to provide informed consent.
  • Pregnancy.
  • Significant coagulopathy that is not correctable.
  • Futility of intervention e.g. pre-terminal patients

结局指标

主要结局

To compare the incidence of stent dysfunction (defined as recurrent jaundice and/or cholangitis) in patients with malignant biliary obstruction receiving FCSEMS vs DPS stent-in-stent through LAMS

时间窗: 26 weeks

次要结局

  • Technical success of LAMS placement.(1 day)
  • Re-intervention rate(26 weeks)
  • Technical success of second stent-in-stent placement(1 day)
  • Clinical success of biliary drainage (evaluated at weeks 1, 2, 4, 12, and 26 using bilirubin and liver enzymes).(weeks 1, 2, 4, 12, and 26)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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