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Continuous Positive Airway Pressure Ventilation After Acute Ischemic Stroke

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

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00151177
Enrollment
100
Registered
2005-09-08
Start date
2005-04-30
Completion date
2008-04-30
Last updated
2010-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Infarction

Keywords

ischemic stroke, CPAP ventilation

Brief summary

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.

Interventions

DEVICECPAP-treatment

night time CPAP-mask ventilation

Sponsors

New Health Sciences, Inc.
CollaboratorINDUSTRY
Rubel GmbH, Heiligenhaus, Germany
CollaboratorUNKNOWN
University Hospital Muenster
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* 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

Design outcomes

Primary

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

Secondary

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

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026