跳至主要内容
临床试验/JPRN-jRCT2091220029
JPRN-jRCT2091220029已完成2 期

A phase II study of talc instillation for the patients with malignant pleural effusions - J-TALC

Hideo Saka, M.D., National Hospital Organization, Nagoya Medical Center0 个研究点目标入组 30 人开始时间: 2009年6月22日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
30

研究概览

简要总结

Effective and safe

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 75age old(—)
性别
All

入选标准

  • 1) Cytologically or histologically proven malignant pleural effusions
  • 2) Symptomatic with malignant pleural effusion and needs intervention
  • 3) Re-expansion of the lung by chest tube drainage
  • 4) Improved symptoms by drainage of pleural effusion
  • 5) Life expectancy of 30 days or more after pleurodesis
  • 6) Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2 after malignant pleural effusion drainage
  • 7) 20 years of age or more, and less than 75 years.
  • 8) Written informed consent from the patient

排除标准

  • 1) Hypersensitive to talc
  • 2) Hypersensitive to lidocaine chloride
  • 3) Severe infection
  • 4) Severe pulmonary emphysema or fibrosis
  • 5) Treatment of active heart failure
  • 6) History of myocardial infarction within 30 days of entry
  • 7) Severe coagulopathy
  • 8) SpO2 less than 90% after drainage
  • 9) Severe pleural adhesion
  • 10) Indication for bilateral pleurodesis
  • 11) History of thoracic surgery like lung resection or pleuro-pulmonary resection on the affected side
  • 12) History of pleurodesis on the affected side
  • 13) Use of systemic corticosteroid and non-steroidal anti-inflammatory agents
  • 14) Pregnant or milk-feeding female, patient who hopes to bear child, or who could not keep contraceptive maneuver
  • 15) Participant of other trial drug study within 6 monthes
  • 16) Inappropriate to enter this trial judged by the physician in charge

研究者

发起方
Hideo Saka, M.D., National Hospital Organization, Nagoya Medical Center

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