跳至主要内容
临床试验/NCT01737775
NCT01737775已完成不适用

Comparative Ultrasonic Study of Post Operative Diaphragmatic Dysfunction in Abdominal and Head and Neck Surgery

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 43 人开始时间: 2012年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
43
试验地点
1
主要终点
Comparison of diaphragmatic amplitude measured by M-Mode ultrasonography performed the day before and the day after surgery in 3 groups: laparoscopic abdominal surgery, abdominal surgery by laparotomy and head and neck surgery.

研究概览

简要总结

Diaphragmatic dysfunction (DD) is one of the main risk factors for post operative respiratory distress syndrome. Ultrasonography is a diagnosis tool for DD but few studies have been published. The aim of this prospective study is to compare the achievement of diaphragmatic function depending on the type of surgery (abdominal and head and neck surgery).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
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
否

入选标准

  • •Age>18 years
  • •Upper abdominal or head and neck surgery
  • •written consent

排除标准

  • •Age <18 years
  • •Pregnancy
  • •History of neuropathy or myopathy,
  • •History of diaphragm paralysis, thoracic surgery, pneumothorax, pneumomediastinum

研究组 & 干预措施

Abdominal laparoscopic surgery (C group)

Experimental

干预措施: Diaphragmatic amplitude measurement (Procedure)

Abdominal surgery by laparotomy (L group)

Experimental

干预措施: Diaphragmatic amplitude measurement (Procedure)

Head and neck surgery (O group)

Experimental

干预措施: Diaphragmatic amplitude measurement (Procedure)

结局指标

主要结局

Comparison of diaphragmatic amplitude measured by M-Mode ultrasonography performed the day before and the day after surgery in 3 groups: laparoscopic abdominal surgery, abdominal surgery by laparotomy and head and neck surgery.

时间窗: two months

次要结局

  • All cause morbidity(within the first 28 days after surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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