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临床试验/NCT03223831
NCT03223831已完成3 期

Partially Covered Versus Uncovered Pyloro-duodenal Stents for Unresectable Malignant Gastric Outlet Obstruction. A Double Blinded Randomised Controlled Trial.

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 116 人开始时间: 2017年8月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
116
试验地点
1
主要终点
Re-intervention rate

研究概览

简要总结

To compare the efficacy of a novel partially covered (PC) versus uncovered (UC) pyloro-duodenal stents (DS) in unresectable malignant gastric outlet obstruction. We hypothesize that the use of PCDS could reduce the re-intervention rates when compared to UCDS.

详细描述

This would be a prospective multi-centred double-blinded randomised controlled study including all patients suffering from malignant gastric outlet obstruction due unresectable primary gastro-duodenal or pancreatico-biliary malignancies. Five international institutions in Hong Kong, Singapore and India would participate in the study.

The procedure would be performed under conscious sedation or monitored anaesthesia. The patients would be randomised PCDS or UCDS after cannulation of the obstruction site is achieved with the guide-wire. The patients or assessors would be blinded to the type of stent that is inserted.

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 (Participant)

盲法说明

Recruited patients would not be informed of the type of stent that was inserted

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

  • Consecutive patients ≥ 18 years old
  • Confirmed unresectable gastro-duodenal or pancreatico-biliary malignancies
  • Suffering from gastric outlet obstruction with a gastric outlet obstruction score of ≤ 1 (appendix 1) 19
  • Performance status ECOG ≤3 (appendix 2)

排除标准

  • Prior metallic stent placement
  • Severe comorbidities precluding the endoscopic procedure (such as cardiopulmonary disease, sepsis, or a bleeding disorder)
  • Life expectancy of less than 1 month
  • History of gastric surgery
  • Linitus plastica
  • Coagulation disorders
  • Pregnancy
  • Unable to give informed consent

结局指标

主要结局

Re-intervention rate

时间窗: 1 year

Percentage of patients requiring additional endoscopic intervention due to stent dysfunction

次要结局

  • Mortality(30 days)
  • Duration of stent patency(1 year)
  • Clinical success(3 days)
  • Adverse events rate(1 year)
  • Gastric outlet obstruction scores (GOOS)(1 year)
  • Stent dysfunction(1 year)
  • Technical success(1 day)
  • Quality of life assessment scores(1 year)

研究者

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

Anthony Teoh

Honorary Associate Professor

Chinese University of Hong Kong

研究点 (1)

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