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Sleep Apnea Treatment After Stroke (SATS)

Primary Purpose

Obstructive Sleep Apnea, Stroke

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
continuous positive airway pressure or CPAP
sham CPAP
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obstructive Sleep Apnea focused on measuring obstructive sleep apnea, stroke, OSA, CPAP, continuous positive airway pressure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Ischemic stroke within 7 days of planned polysomnography/sleep screening study Modified Rankin Scale score >1 If of child-bearing potential, has a negative urine or serum pregnancy test Exclusion Criteria: Decompensated heart failure Cardiac or respiratory arrest within the past 3 months Myocardial infarction within the past 3 months Severe pneumonia Hypertension refractory to treatment Any other unstable medical condition which is thought to interfere with participation Known preexisting OSA already on CPAP or previously failed CPAP or used CPAP Previous pneumothorax Bullous emphysema Chronic obstructive pulmonary disease (COPD), obesity-hypoventilation, or another condition warranting the use of nasal bilevel positive airway pressure instead of CPAP Acute sinus or ear infection

Sites / Locations

  • University of Michigan

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

1

2

Arm Description

CPAP

sham CPAP (placebo)

Outcomes

Primary Outcome Measures

Cumulative Continuous Positive Airway Pressure (CPAP)/Sham CPAP Usage Hours Over the 3 Month Period.
Number of Subjects Who Withdraw From Study.
Prespecified outcome.

Secondary Outcome Measures

Barthel Index
Barthel Index score range: 0 (worst, fully dependent) - 100 (best, independent).

Full Information

First Posted
January 26, 2006
Last Updated
January 31, 2013
Sponsor
University of Michigan
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1. Study Identification

Unique Protocol Identification Number
NCT00282815
Brief Title
Sleep Apnea Treatment After Stroke (SATS)
Official Title
Treatment of Obstructive Sleep Apnea After Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
December 2012
Overall Recruitment Status
Terminated
Why Stopped
Poor recruitment. Funding expired.
Study Start Date
September 2004 (undefined)
Primary Completion Date
May 2010 (Actual)
Study Completion Date
May 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine if treating stroke patients who have obstructive sleep apnea with continuous positive airway pressure will improve symptoms caused by the stroke.
Detailed Description
Stroke is the leading cause of adult disability in the United States, yet there are very few treatments that improve stroke outcome. Obstructive sleep apnea (OSA)--frequent upper airway blockage that occurs during sleep--is common after stroke, affecting more than half of stroke patients. The most common treatment for obstructive sleep apnea in the general population is nasal continuous positive airway pressure (CPAP) applied through a nasal mask during the hours of sleep. Positive air pressure holds the naso-oro-pharyngeal airway open during sleep. The objective of this single-center, prospective, randomized study is to evaluate CPAP treatment in post-stroke patients. Participants will go through a medical interview, a brief neurological examination, and a sleep study to screen them for OSA. Those with OSA will be eligible for the second phase of the study during which participants will be randomly selected to receive either treatment with CPAP or with sham CPAP (placebo). This project promises to establish feasibility, develop design and identify suitable outcome measures (e.g. hours of CPAP treatment per week, functional outcome, depression, fatigue, and impaired alertness) for a large-scale clinical trial of CPAP in stroke patients with OSA. If the larger trial shows benefits of CPAP, a new treatment for more than half of all stroke patients will become available.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea, Stroke
Keywords
obstructive sleep apnea, stroke, OSA, CPAP, continuous positive airway pressure

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
CPAP
Arm Title
2
Arm Type
Sham Comparator
Arm Description
sham CPAP (placebo)
Intervention Type
Device
Intervention Name(s)
continuous positive airway pressure or CPAP
Intervention Description
RemStar Pro (Respironics, Inc.) The CPAP is applied through a nasal mask during the hours of sleep. Positive air pressure holds the naso-oro-pharyngeal airway open during sleep.
Intervention Type
Device
Intervention Name(s)
sham CPAP
Intervention Description
sham CPAP
Primary Outcome Measure Information:
Title
Cumulative Continuous Positive Airway Pressure (CPAP)/Sham CPAP Usage Hours Over the 3 Month Period.
Time Frame
3 months
Title
Number of Subjects Who Withdraw From Study.
Description
Prespecified outcome.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Barthel Index
Description
Barthel Index score range: 0 (worst, fully dependent) - 100 (best, independent).
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ischemic stroke within 7 days of planned polysomnography/sleep screening study Modified Rankin Scale score >1 If of child-bearing potential, has a negative urine or serum pregnancy test Exclusion Criteria: Decompensated heart failure Cardiac or respiratory arrest within the past 3 months Myocardial infarction within the past 3 months Severe pneumonia Hypertension refractory to treatment Any other unstable medical condition which is thought to interfere with participation Known preexisting OSA already on CPAP or previously failed CPAP or used CPAP Previous pneumothorax Bullous emphysema Chronic obstructive pulmonary disease (COPD), obesity-hypoventilation, or another condition warranting the use of nasal bilevel positive airway pressure instead of CPAP Acute sinus or ear infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Devin Brown, MD, MS
Organizational Affiliation
Associate Professor, Stroke Program, University of Michigan
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lewis Morgenstern, MD
Organizational Affiliation
Director, Stroke Program, University of Michigan
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jack Kalbfleisch, PhD
Organizational Affiliation
University of Michigan Dept of Biostatistics
Official's Role
Study Director
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21784661
Citation
Brown DL, Chervin RD, Kalbfleisch JD, Zupancic MJ, Migda EM, Svatikova A, Concannon M, Martin C, Weatherwax KJ, Morgenstern LB. Sleep apnea treatment after stroke (SATS) trial: is it feasible? J Stroke Cerebrovasc Dis. 2013 Nov;22(8):1216-24. doi: 10.1016/j.jstrokecerebrovasdis.2011.06.010. Epub 2011 Jul 23.
Results Reference
result

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Sleep Apnea Treatment After Stroke (SATS)

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