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Clinical Trials/NCT01561677
NCT01561677UnknownNot Applicable

Consequences of Obstructive Sleep Apnea Syndrome (OSAS) on the Outcome and the Survival After Ischemic Subtentorial Stroke. Impact of the Treatment With Continuous Positive Airway Pressure (CPAP)

University Hospital, Montpellier1 site in 1 country300 target enrollmentStarted: September 1, 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
300
Locations
1
Primary Endpoint
functional independence scale

Study Overview

Brief Summary

Obstructive Sleep Apnea Syndrome (OSAS) is associated with stroke as a risk factor but little is known about the consequences of OSAS on the outcome and the survival after stroke. The aim of the investigators study is first to evaluate the outcome and the survival of patients with stroke depending of OSAS (presence and severity of OSAS) and second to compare the outcome and survival of patients with severe OSAS depending on the treatment of the syndrome with nocturnal continuous positive airway pressure. The investigators hypothesis is that OSAS is associated with worst survival and outcome and needs to be treated at the subacute phase of stroke.

Detailed Description

Objective

The aim of our study is to evaluate the consequences of obstructive sleep apnea syndrome on the functional outcome and the survival after an ischemic stroke and to measure the impact of the treatment with continuous positive airway pressure on the outcome of patients with severe obstructive sleep apnea syndrome.Patients and methods : We will prospectively explore by polysomnography, 300 consecutive patients hospitalized for an ischemic stroke in the stroke units of university hospitals at the sub acute phase after stroke (J15±4). 1) We will compare the functional outcome, the neurological impairment, the peripheral endothelial function, the continuous blood pressure measure on 24 hours recording, the quality of life and the survival at 3, 6 and 12 months in four groups of patients depending on their apnea/hypopnea index 2) In patients with severe obstructive sleep apnea syndrome, we will explore the impact on the functional outcome, the neurological impairment, and the survival at 3, 6 et 12 months of a treatment with continuous positive airway pressure (CPAP) randomly compared to a treatment with sham CPAP (non efficacious pressure) during 3 months. Conclusion : This study should allow us to evaluate the consequences of obstructive sleep apnea syndrome on the outcome and the survival after ischemic stroke and the impact and the tolerance of the treatment with continuous positive airway pressure in patients with severe obstructive sleep apnea syndrome.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Double (Participant, Care Provider)

Eligibility Criteria

Ages
18 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Brain infarction confirmed by brain imaging
  • •follow up possible
  • •Severity at admission and at one week follow up:
  • •NIHSS ≥ 4 or- isolated aphasia (item 9 ofNIHSS ≥ 1) or
  • •negligence (item 11 du NIHSS ≥ 2) or
  • •distal motor deficit (score ≥ 1)
  • •Health insurance affiliation
  • •Inform and free consent agreement

Exclusion Criteria

  • Not provided

Arms & Interventions

apnea/hypopnea index (AHI<5 : no OSAS)

No Intervention

apnea/hypopnea index (5≥AHI<15 : mild OSAS)

No Intervention

apnea/hypopnea index (15≤AHI<30 :moderate OSAS)

No Intervention

apnea/hypopnea index ( AHI≥30 : severe OSAS treated).

Active Comparator

Treated with CPAP

Intervention: Continuous Positive Airway pressure-RESPIRONICS (Device)

apnea/hypopnea index ( AHI≥30:severe OSAS untreated).

Sham Comparator

Treated with sham CPAP (placebo)

Intervention: Sham Continuous Positive Airway pressure-RESPIRONICS (Device)

Outcomes

Primary Outcomes

functional independence scale

Time Frame: 3 months

The variation of the functional independence scale is evaluated by the Barthel Index at three months after stroke in four groups of patients depending on their apnea/hypopnea.In the patients group severe OSAS treated with CPAP from day 15 after stroke compared to patients with severe OSAS treated with sham CPAPThe neurological dependency will be evaluated by the Barthel Index .This scale measures the consequences of the motor and cognitive disorders on the daily living with 10 items.

Secondary Outcomes

  • the quality of life(3 months)
  • blood pressure(3 months)
  • neurological impairment(3 months)
  • the handicap(3 months)
  • the survival(3 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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