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临床试验/NCT02931617
NCT02931617已完成不适用

Comparison of Two Modes of Respiratory Physiotherapy in Cardio-thoracic Surgical Patients

Tampere University Hospital1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2013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
120
试验地点
1
主要终点
Number of patients with atelectasis

研究概览

简要总结

Two forms of pre and postoperative physiotherapy are compared in three cohorts of patients undergoing cardio-thoracic surgery: Minor thoracic surgery (biopsy), major thoracic surgery (lobectomy etc, open or VATS) and cardiac surgery

详细描述

Inspiratory force calibrated training is applied in a controlled randomized trial

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
16 Years 至 99 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •cardiothoracic operation,
  • •informed consent

排除标准

  • •reduced co-operation (such as psychiatric diagnosis),
  • •severe neurologic disease affecting respiratory function,
  • •alcohol or drug abuse at hospital entry,
  • •tuberculosis or other contagious lung infection,
  • •severe respiratory insufficiency SpO2 < 90 or blood pO2 <8 or rep.rate > 25/min at rest or supplementary oxygen required at home,
  • •cardiac pacemaker.

研究组 & 干预措施

Physiotherapy w/Positive end expiratory pressure training

Active Comparator

Chest Physiotherapy w/Positive end expiratory pressure training; post therapy lung volume measurements

干预措施: Chest Physiotherapy (Other)

Physiotherapy w/Positive end expiratory pressure training

Active Comparator

Chest Physiotherapy w/Positive end expiratory pressure training; post therapy lung volume measurements

干预措施: Post-therapy lung volume measurements (Device)

Physiotherapy w/Inspiratory force training

Experimental

Chest Physiotherapy w/Inspiratory force training; post therapy lung volume measurements

干预措施: Chest Physiotherapy (Other)

Physiotherapy w/Inspiratory force training

Experimental

Chest Physiotherapy w/Inspiratory force training; post therapy lung volume measurements

干预措施: Post-therapy lung volume measurements (Device)

结局指标

主要结局

Number of patients with atelectasis

时间窗: Preop + 1-3 postoperative days

In chest x-ray

Change in peripheral oxygen saturation

时间窗: Preop + 1-3 postoperative days

Serial measurements

Postoperative lung complications

时间窗: Preop + 1-30 postoperative days

Number of patients with lung infections, prolonged air leak, pneumothorax

Change in FEV1

时间窗: Preop + 1-3 postoperative days

Serial measurements

次要结局

  • Compliance to Chest physiotherapy(Preop + 1-3 postoperative days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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