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Sleep Disordered Breathing in Transient Ischemic Attack (TIA)/Ischemic Stroke and Continuous Positive Airway Pressure (CPAP) Treatment Efficacy (SAS-CARE)

Primary Purpose

TIA, Ischemic Stroke

Status
Unknown status
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
CPAP
Sponsored by
Prof. Claudio Bassetti
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for TIA focused on measuring Sleep disordered breathing, Continuous Positive Airway Pressure, Sleep apnoea, Markers of atherosclerosis

Eligibility Criteria

35 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ≥ 35 years old and < 75 years old
  • with clinical diagnosis of TIA or ischemic stroke
  • admitted in a Stroke Unit within 2 days from onset of symptoms
  • or with TIA or ischemic stroke within the last 60-90 days
  • signed Informed Consent

Exclusion Criteria:

  • with unstable clinical situation (cardio-respiratory or life-threatening medical conditions)
  • currently on CPAP or on CPAP during the last 3 months before stroke
  • with non-ischemic events (intracerebral/subarachnoid haemorrhage)
  • Patients with coma/stupor
  • with borderline obstructive SDB (AHI 10-19)
  • with any condition that interferes with the acceptance of CPAP treatment

Sites / Locations

  • University Hospital Münster
  • Dipartimento Neuroscienze, Ospedale Niguarda
  • Ospedale San Giovanni
  • Neurocenter of Southern Switzerland, Ospedale Civico
  • Inselspital, Universitätsklinik für Pneumologie

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

No Intervention

Active Comparator

Arm Label

CPAP in sleepy patients with SDB

no CPAP in non sleepy patients with SDB

CPAP in non sleepy patients with SDB

Arm Description

SDB defined as AHI >=20 Sleepy defined as Epworth Sleepiness Score >=10

SDB defined as AHI >=20 Sleepy defined as Epworth Sleepiness Score >=10

SDB defined as AHI >=20 Sleepy defined as Epworth Sleepiness Score >=10

Outcomes

Primary Outcome Measures

Occurence of new vascular events or death in stroke survivors (myocardial infarction, stroke, death) assessed by telephone or reported
New vascular events will be assessed by regular telephone interviews at 6,12 and 24 months after stroke

Secondary Outcome Measures

CPAP-Compliance measured by hours of usage
Compliance is monitored for the use of the CPAP by the pulmonary specialist at the patients' routine visits 2-3, 4-6 weeks, 3-6 months, 12 and 24 months after randomisation. The hours ofuse are registered by a chip inserted in the device. Good compliance is, if the device was used > 10 hours per day. Satisfactory compliance is defined for a use of the CPAP for at least 4 hours per night during at least 70% of the nights. Insufficient compliance is defined as < 4 hours per night or less than 70% of nights.
Blood pressure profile (systolic mean, diastolic mean, max, min: general, day, night) measured in mmHg for every patient by ambulatory 24h-BP-devices in the acute stroke phase, after 3 months and after 12 months
Mean systolic and diastolic BP values, minimal and maximum values will be calculated for each patient for each period of time [after stroke: whole measuring period, (36 h) first night, second day, and second night after stroke; 3 months after stroke: whole period (24 h), day, night]. In addition same measurements will be made 12 months after stroke The occurrence of dippers will be registered at baseline (after stroke) and at 3 months. A dipper is defined, if the mean pressure at night is diminished more than 10% (compared to day data). An inverse-dipper is defined if more than 10% augmentation of night pressure will be registered. A deep-deeper is defined the mean pressure at night is diminished more than 20% (compared to day data).
Blood pressure dipping measured by ambulatory 24h-BP-devices in the acute stroke phase, after 3 months and after 12 months
The occurrence of dippers will be registered at baseline (after stroke) and at 3 months and 12 months after stroke. A dipper is defined, if the mean pressure at night is diminished more than 10% (compared to day data). An inverse-dipper is defined if more than 10% augmentation of night pressure will be registered. A deep-deeper is defined the mean pressure at night is diminished more than 20% (compared to day data).

Full Information

First Posted
April 1, 2010
Last Updated
October 23, 2015
Sponsor
Prof. Claudio Bassetti
Collaborators
Swiss National Science Foundation, Schweizerische Herzstiftung, ResMed, Philips Respironics
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1. Study Identification

Unique Protocol Identification Number
NCT01097967
Brief Title
Sleep Disordered Breathing in Transient Ischemic Attack (TIA)/Ischemic Stroke and Continuous Positive Airway Pressure (CPAP) Treatment Efficacy
Acronym
SAS-CARE
Official Title
Sleep Disordered Breathing in TIA/Ischemic Stroke: Effects on Short- and Long-term Outcome and CPAP Treatment Efficacy: an Open, Observational, Clinical, Multicentre Trial With a Randomized Arm
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Unknown status
Study Start Date
July 2010 (undefined)
Primary Completion Date
April 2016 (Anticipated)
Study Completion Date
April 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Prof. Claudio Bassetti
Collaborators
Swiss National Science Foundation, Schweizerische Herzstiftung, ResMed, Philips Respironics

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study aims to observe the short term effect (3-month) of sleep disordered breathing (SDB) on cardiovascular parameters, heart rate variability, endothelial function and surrogate markers of atherosclerosis after acute cerebrovascular events (ACE). The long-term effect (6-24-month) of Continuous Positive Airway Pressure (CPAP) on clinical vascular outcome, cardiovascular parameters, evolution of surrogate of atherosclerosis heart rate variability and endothelial function after ACE is observed over 24 months. A preventive effect of CPAP therapy on cerebro-vascular events in patients with moderate-severe obstructive SDB without sleepiness after ictus or transient ischaemic attack will be evaluated.
Detailed Description
Sleep disordered breathing is an independent risk factor for cardiovascular morbidity and mortality and is frequent in patients with acute cerebrovascular events. In this study the investigators observe the association between sleep disordered breathing, hypertension, stroke and the evolution of blood markers for atherosclerosis as well as the efficacy of Continuous Positive Airway Pressure treatment in patients with acute or subacute cerebrovascular events. Sleep disordered breathing is an independent risk factor for cardiovascular morbidity and mortality and is frequent in patients with acute cerebrovascular events. In this study the investigators observe the association between sleep disordered breathing, hypertension, stroke and the evolution of blood markers for atherosclerosis as well as the efficacy of Continuous Positive Airway Pressure treatment in patients with acute or subacute cerebrovascular events. The SAS CARE 1 study is planned to verify whether or not sleep disordered breathing has a detrimental 3 months effect on cardiovascular functions and markers after acute cerebrovascular events. The SAS CARE 2 study is designed to address whether or not the treatment of sleep disordered breathing with CPAP reduces the combined rate of mortality, stroke, cardiovascular events (myocardial infarction/revascularisation/instable angina/ hospitalisation for heart insufficiency) over a 24 months period in patients after acute cerebrovascular events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
TIA, Ischemic Stroke
Keywords
Sleep disordered breathing, Continuous Positive Airway Pressure, Sleep apnoea, Markers of atherosclerosis

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
246 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CPAP in sleepy patients with SDB
Arm Type
Active Comparator
Arm Description
SDB defined as AHI >=20 Sleepy defined as Epworth Sleepiness Score >=10
Arm Title
no CPAP in non sleepy patients with SDB
Arm Type
No Intervention
Arm Description
SDB defined as AHI >=20 Sleepy defined as Epworth Sleepiness Score >=10
Arm Title
CPAP in non sleepy patients with SDB
Arm Type
Active Comparator
Arm Description
SDB defined as AHI >=20 Sleepy defined as Epworth Sleepiness Score >=10
Intervention Type
Other
Intervention Name(s)
CPAP
Primary Outcome Measure Information:
Title
Occurence of new vascular events or death in stroke survivors (myocardial infarction, stroke, death) assessed by telephone or reported
Description
New vascular events will be assessed by regular telephone interviews at 6,12 and 24 months after stroke
Time Frame
24 monts after stroke
Secondary Outcome Measure Information:
Title
CPAP-Compliance measured by hours of usage
Description
Compliance is monitored for the use of the CPAP by the pulmonary specialist at the patients' routine visits 2-3, 4-6 weeks, 3-6 months, 12 and 24 months after randomisation. The hours ofuse are registered by a chip inserted in the device. Good compliance is, if the device was used > 10 hours per day. Satisfactory compliance is defined for a use of the CPAP for at least 4 hours per night during at least 70% of the nights. Insufficient compliance is defined as < 4 hours per night or less than 70% of nights.
Time Frame
up to 24 months after stroke
Title
Blood pressure profile (systolic mean, diastolic mean, max, min: general, day, night) measured in mmHg for every patient by ambulatory 24h-BP-devices in the acute stroke phase, after 3 months and after 12 months
Description
Mean systolic and diastolic BP values, minimal and maximum values will be calculated for each patient for each period of time [after stroke: whole measuring period, (36 h) first night, second day, and second night after stroke; 3 months after stroke: whole period (24 h), day, night]. In addition same measurements will be made 12 months after stroke The occurrence of dippers will be registered at baseline (after stroke) and at 3 months. A dipper is defined, if the mean pressure at night is diminished more than 10% (compared to day data). An inverse-dipper is defined if more than 10% augmentation of night pressure will be registered. A deep-deeper is defined the mean pressure at night is diminished more than 20% (compared to day data).
Time Frame
up to 12 months after stroke
Title
Blood pressure dipping measured by ambulatory 24h-BP-devices in the acute stroke phase, after 3 months and after 12 months
Description
The occurrence of dippers will be registered at baseline (after stroke) and at 3 months and 12 months after stroke. A dipper is defined, if the mean pressure at night is diminished more than 10% (compared to day data). An inverse-dipper is defined if more than 10% augmentation of night pressure will be registered. A deep-deeper is defined the mean pressure at night is diminished more than 20% (compared to day data).
Time Frame
up to 12 months after stroke

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥ 35 years old and < 75 years old with clinical diagnosis of TIA or ischemic stroke admitted in a Stroke Unit within 2 days from onset of symptoms or with TIA or ischemic stroke within the last 60-90 days signed Informed Consent Exclusion Criteria: with unstable clinical situation (cardio-respiratory or life-threatening medical conditions) currently on CPAP or on CPAP during the last 3 months before stroke with non-ischemic events (intracerebral/subarachnoid haemorrhage) Patients with coma/stupor with borderline obstructive SDB (AHI 10-19) with any condition that interferes with the acceptance of CPAP treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudio Bassetti, Professor
Organizational Affiliation
Universitätsspital Bern (Inselspital) und Universität Bern
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Carlo Cereda, Capo CLinica
Organizational Affiliation
Neurocentre of Southern Switzerland, Ospedale Civico
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Sebastian Ott, MD
Organizational Affiliation
Pneumology, University Hospital, Bern
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Lino Nobili, Prof. MD
Organizational Affiliation
Neurology, Stroke Unit, Ospedale Niguarda, Milan, Italy
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mauro Manconi, MD
Organizational Affiliation
Neurocentre of Southern Switzerland, Ospedale Civico
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Peter Young, Prof. MD
Organizational Affiliation
Universitätsklinik Münster, Zentrum für Schlafmedizin
Official's Role
Study Chair
Facility Information:
Facility Name
University Hospital Münster
City
Münster
Country
Germany
Facility Name
Dipartimento Neuroscienze, Ospedale Niguarda
City
Milan
State/Province
Lombardia
ZIP/Postal Code
I-20162
Country
Italy
Facility Name
Ospedale San Giovanni
City
Bellinzona
State/Province
Ticino
ZIP/Postal Code
CH-6500
Country
Switzerland
Facility Name
Neurocenter of Southern Switzerland, Ospedale Civico
City
Lugano
State/Province
Ticino
ZIP/Postal Code
CH-6900
Country
Switzerland
Facility Name
Inselspital, Universitätsklinik für Pneumologie
City
Bern
ZIP/Postal Code
CH-3010
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
8909424
Citation
Bassetti C, Aldrich MS, Chervin RD, Quint D. Sleep apnea in patients with transient ischemic attack and stroke: a prospective study of 59 patients. Neurology. 1996 Nov;47(5):1167-73. doi: 10.1212/wnl.47.5.1167.
Results Reference
background
PubMed Identifier
10201066
Citation
Bassetti C, Aldrich MS. Sleep apnea in acute cerebrovascular diseases: final report on 128 patients. Sleep. 1999 Mar 15;22(2):217-23. doi: 10.1093/sleep/22.2.217.
Results Reference
background
PubMed Identifier
15781100
Citation
Marin JM, Carrizo SJ, Vicente E, Agusti AG. Long-term cardiovascular outcomes in men with obstructive sleep apnoea-hypopnoea with or without treatment with continuous positive airway pressure: an observational study. Lancet. 2005 Mar 19-25;365(9464):1046-53. doi: 10.1016/S0140-6736(05)71141-7.
Results Reference
background
PubMed Identifier
16543515
Citation
Bassetti CL, Milanova M, Gugger M. Sleep-disordered breathing and acute ischemic stroke: diagnosis, risk factors, treatment, evolution, and long-term clinical outcome. Stroke. 2006 Apr;37(4):967-72. doi: 10.1161/01.STR.0000208215.49243.c3. Epub 2006 Mar 16.
Results Reference
background
PubMed Identifier
19406983
Citation
Martinez-Garcia MA, Soler-Cataluna JJ, Ejarque-Martinez L, Soriano Y, Roman-Sanchez P, Illa FB, Canal JM, Duran-Cantolla J. Continuous positive airway pressure treatment reduces mortality in patients with ischemic stroke and obstructive sleep apnea: a 5-year follow-up study. Am J Respir Crit Care Med. 2009 Jul 1;180(1):36-41. doi: 10.1164/rccm.200808-1341OC. Epub 2009 Apr 30.
Results Reference
background
PubMed Identifier
30032306
Citation
Pace M, Camilo MR, Seiler A, Duss SB, Mathis J, Manconi M, Bassetti CL. Rapid eye movements sleep as a predictor of functional outcome after stroke: a translational study. Sleep. 2018 Oct 1;41(10). doi: 10.1093/sleep/zsy138.
Results Reference
derived
PubMed Identifier
24435018
Citation
Manconi M, Zavalko I, Cereda C, Pisarenco I, Ott S, Fulda S, Bassetti CL. Longitudinal polysomnographic assessment from acute to subacute phase in infratentorial versus supratentorial stroke. Cerebrovasc Dis. 2014;37(2):85-93. doi: 10.1159/000356323. Epub 2014 Jan 16.
Results Reference
derived
PubMed Identifier
22812731
Citation
Cereda CW, Petrini L, Azzola A, Ciccone A, Fischer U, Gallino A, Gyorik S, Gugger M, Mattis J, Lavie L, Limoni C, Nobili L, Manconi M, Ott S, Pons M, Bassetti CL. Sleep-disordered breathing in acute ischemic stroke and transient ischemic attack: effects on short- and long-term outcome and efficacy of treatment with continuous positive airways pressure--rationale and design of the SAS CARE study. Int J Stroke. 2012 Oct;7(7):597-603. doi: 10.1111/j.1747-4949.2012.00836.x. Epub 2012 Jul 19.
Results Reference
derived
Links:
URL
http://www.eoc.ch
Description
Click here to see more information about our hospital
URL
http://www.swissheart.ch
Description
provides financial support for the study

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Sleep Disordered Breathing in Transient Ischemic Attack (TIA)/Ischemic Stroke and Continuous Positive Airway Pressure (CPAP) Treatment Efficacy

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