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临床试验/NCT00655928
NCT00655928已完成2 期

Modulation of Lung Injury Complicating Lung Resection

Imperial College London1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2007年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
52
试验地点
1
主要终点
Post-operative Plasma IL-6

研究概览

简要总结

The purpose of this study is to determine whether N-acetylcysteine given intravenously 1 day pre-operatively is effective in preventing inflammation in the lungs, as measured by tests on blood, breath and lung specimens, in patients undergoing surgery to remove a portion of lung.

详细描述

Acute lung injury occurs following lung resection in about 5% cases, and has a high mortality of around 50%. Management of these patients is largely supportive. Even in patients who do not develop clinical evidence of acute lung injury, markers of inflammation and oxidative stress are present in blood and exhaled breath condensate after lung resection. The purpose of this randomised double-blind placebo-controlled study is to determine whether lung injury can be prevented by pre-administration of N-acetylcysteine.

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
Quadruple (Participant, Care Provider, Investigator, 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

  • Elective lung resection for cancer

排除标准

  • Age less than 18 years
  • Women of child-bearing age or potential
  • Known allergy to N-acetylcysteine
  • Oral steroid in the preceding 1 month
  • N-acetylcysteine in the preceding 1 month
  • Unable to receive standardised anaesthetic approach

研究组 & 干预措施

N-acetylcysteine

Experimental

Participant received N-acetylcysteine 240mg/kg in 1 litre 0.9% saline intravenous over 12 hours pre-operatively

干预措施: N-acetylcysteine (Drug)

Placebo

Placebo Comparator

Participant received 0.9% saline 1 litre intravenous over 12 hours pre-operatively

干预措施: 0.9% saline (Drug)

结局指标

主要结局

Post-operative Plasma IL-6

时间窗: Post operative, 24 hours

Plasma IL-6 was measured in duplicate using ELISA.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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