跳至主要内容
临床试验/NCT00151177
NCT00151177已完成1 期

Feasibility and Efficacy Study of Early Continuous Positive Airway Pressure Ventilation in Patients With Acute Ischemic Stroke

University Hospital Muenster2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2005年4月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
100
试验地点
2
主要终点
Primary endpoint is to test the feasibility of early non-invasive CPAP ventilation in acute stroke patients

研究概览

简要总结

More than half of all stroke patients have sleep apneas in the acute phase after stroke. Sleep apneas may be associated with higher degrees of disability three months after stroke due to numerous factors associated with sleep apneas such as persistent hypertension, cardiac arrhythmias, and clotting disorders.

Non-invasive CPAP (continuous positive airway pressure)-therapy may reverse a number of these effects very shortly after initiation. The aim of the study is to test the feasibility of early non-invasive CPAP treatment starting in the first night after stroke onset, and to test its efficacy in a randomized clinical trial.

50 patients with acute ischemic stroke will be enrolled and randomly assigned to standard care PLUS CPAP treatment or standard care only. All patients randomized to the intervention group will receive CPAP therapy for the first three nights after stroke. In the fourth night, a cardiorespiratory polygraphy will be performed in patients and controls. Patients assigned to the intervention group with a respiratory distress index > 10/h will be treated further on. On admission, day 4, and day 10 after stroke, diffusion weighted MRI imaging will be performed to determine the size of the infarction. The NIHSS score will be used to assess clinical short-term outcome on day 4 and day 10. After three months, the outcome will be determined using the modified Rankin scale.

As CPAP therapy may be more laborious for the provider, the additional work-load will be documented using pre-specified scales.

Primary hypothesis of the study is, that CPAP therapy is feasible in acute stroke patients and that the additional work load will not outweigh the benefits.

Secondary hypothesis is that patients assigned to the treatment group have smaller infarctions on MRI and less neurological deficits at 3 months after stroke.

Patients entering the study will be investigated by transcranial Doppler ultrasound in case they have sufficient temporal bone windows for insonation and no stenosis or occlusions of major brain supplying arteries by the time of investigation that disturb the intracerebral blood flow.

All intracranial arteries will be assessed before treatment, after treatment and on day 8 after the insult.

Screen shots will be taken and will be analysed by dynamic vascular ultrasound (DVA), a new software algorithm developed by NHSi, to investigate microcirculatory information from the flow spectra of the major intracranial arteries.

The data from this post-hoc analysis are compared with the data of the polysomnography and with treatment.

Primary hypothesis in this substudy is that DVA reliably identifies patients with sleep apnea on days one and four after stroke. Secondary hypothesis is that DVA can distinguish between treated patients and controls.

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
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • AGE 18-85 years,
  • NIH-SS 2-20 points,
  • NIH-SS subitem 1a <=1.

排除标准

  • Modified Rankin Scale Score >=2 on admission
  • primary intubation,
  • Congestive heart failure (NYHA >=3),
  • respiratory insufficiency
  • recurrent vomiting
  • absence of gag reflex,
  • participation in another RCT
  • for the ultrasound sub-study
  • absence of temporal bone window for insonation
  • stenosis or occlusion of major brain supplying arteries interfering with normal blood flow

结局指标

主要结局

Primary endpoint is to test the feasibility of early non-invasive CPAP ventilation in acute stroke patients

次要结局

  • Disability measured by the modified Rankin scale after three months
  • Size of brain infarction on diffusion weighted MRI imaging at day 10 after symptom onset

研究者

发起方
University Hospital Muenster
申办方类型
Other

研究点 (2)

Loading locations...

相似试验