跳至主要内容
临床试验/NCT04626180
NCT04626180已完成不适用

Effects of Pre-extubation Manual Hyper Inflation in Comparison to Regular Extubation Following Sternotomy.

Foundation University Islamabad1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2017年9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
54
试验地点
1
主要终点
Oxygen saturation

研究概览

简要总结

Post operative pulmonary complication (PPC) is one of the cause of mortality and morbidity after sternotomy. There is no accessible confirmation which shows the impact of Pre Extubation Manual Hyperinflation method with Regular Extubation procedure. After sternotomy manual hyperinflation technique is not taken during extubation. The objective of the study was to determine the effect of Pre Extubation Manual Hyperinflation technique VS regular Extubation technique on vitals and respiratory parameters in patients after Sternotomy.

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
Double (Participant, Investigator)

入排标准

年龄范围
40 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age 40 to 60
  • •Patient undergone surgery (sternotomy)
  • •Elective intubated (ETT orally)
  • •Ventilated more than 3 hours -

排除标准

  • •Patient with any neurological issue (mentally disturbed) who cannot understand the command
  • •Complicated extubation
  • •Pulmonary pathology where lung hyperinflation was contra-indicated (e.g. acute respiratory distress syndrome, undrained pneumothorax or exacerbation of chronic obstructive pulmonary disease and acute pulmonary edema.
  • •Raised intracranial pressure
  • •Redo or reopen. -

研究组 & 干预措施

Pre Extubation Manual Hyperinflation

Experimental

干预措施: Manual Hyperinflation (Procedure)

Regular Extubation

Active Comparator

干预措施: Extubation (Procedure)

Pre Extubation Manual Hyperinflation

Experimental

干预措施: Extubation (Procedure)

结局指标

主要结局

Oxygen saturation

时间窗: 1 day

Peak expiratory flow rate

时间窗: 1 day

Forced vital capacity

时间窗: 1 day

Blood pCO2

时间窗: 1 day

Blood pHCO3

时间窗: 1 day

Blood pH

时间窗: 1 day

Blood pO2

时间窗: 1 day

Pulse rate

时间窗: 1 day

Forced expiratory volume

时间窗: 1 day

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)

Loading locations...

相似试验