跳至主要内容
临床试验/NCT04472468
NCT04472468终止不适用

Primary Percutaneous Pericardiotomy for Malignant Pericardial Effusion (PMAP) - a Randomized Study

Chinese University of Hong Kong2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2020年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
50
试验地点
2
主要终点
Procedural related complications

研究概览

简要总结

Pericardial effusion is a common complication in patients with metastatic malignancy. While pericardiocentesis provide effective relieve from life-threatening situation such as cardiac tamponade, recurrence of pericardial effusion after pericardiocentesis is common. We hypothesize that percutaneous balloon pericardiotomy in addition to standard pericardiocentesis with prolonged drainage can prevent pericardial effusion recurrence in patients with malignant pericardial effusion.

详细描述

Pericardial effusion is a common complication in patients with metastatic malignancy with an incidence as high as 21%. The occurrence of malignant pericardial effusion significantly impacts on patient's survival and quality of life. While pericardiocentesis provide effective relieve from life-threatening situation such as cardiac tamponade, recurrence of pericardial effusion after pericardiocentesis is common and occurs in as high as 31% of patients. Retrospective data has shown that prolonged pericardial drainage might reduce the recurrence rate but at the cost of increased risk of infection and prolonged hospital stay. Surgical pericardiotomy was used in the past but was not shown to reduce recurrence over prolonged pericardial drainage and is associated with a higher rate of complications. Surgical pericardial window creation via a mini-thoracotomy might be an effective treatment and can be considered in patient with pericardial tamponade. The safety and feasibility of Percutaneous Balloon pericardiotomy (PBP) has been first described 1993 and has been shown to be an alternative treatment for patient with malignant pericardial effusion. However, no data is available on the efficacy of PBP in reducing the recurrence of pericardial effusion, in comparison with standard pericardiocentesis with prolonged drainage. We aim to perform a single centre, randomized, prospective, open label controlled pragmatic trial to compare percutaneous balloon pericardiotomy (treatment) to standard pericardiocentesis with prolonged drainage (control) in preventing pericardial effusion recurrence in patients with malignant pericardial effusion.

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

入选标准

  • Patients with confirmed active malignancy AND,
  • Presence of at least moderate (>10cm) pericardial effusion on CT or Echocardiography

排除标准

  • Patients unable to give an informed consent,
  • Previous history of open-heart surgery
  • Previous history of pericardial window or pericardial instillation of sclerosing therapy.
  • Scheduled thoracic or cardiac surgery within the next 3 months
  • Patients with contraindications for endovascular procedure such as disseminated intravascular coagulopathy or significant ongoing bleeding tendency, and systemic septicaemia.
  • Patient with small or loculated pericardial effusion that is not accessible by subxiphoid approach.

结局指标

主要结局

Procedural related complications

时间窗: Immediate after intervention

Procedural related complications including procedural related death, need for urgent surgical intervention, pleural effusion and pneumothorax

Pericardial effusion recurrence

时间窗: 3 months

Recurrence of pericardial effusion after index procedure, defined as development of moderate or more pericardial effusion (\>10mm) on follow-up imaging.

次要结局

  • Pericardial effusion free survival(3 months)
  • Pericardial drain indwelling time(during index procedure)
  • Catheter tract tumor seeding(3 months)
  • Ascites/Pleural effusion(3 months)
  • Survival(3 months)
  • cardiac tamponade(3 months)
  • Quality of life measure (using Functional Assessment of Cancer Therapy - General version (Chinese version)).(3 months)

研究者

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

GuangMing Tan

Honorary Clinical Assistant Professor

Chinese University of Hong Kong

研究点 (2)

Loading locations...

相似试验