Status:
WITHDRAWN
Evaluation of Obstructive Sleep Apnea (OSA) Using Portable Sleep Testing (PST) Devices on an Inpatient Stroke Unit
Lead Sponsor:
Wake Forest University Health Sciences
Conditions:
Obstructive Sleep Apnea
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to evaluate the feasibility of testing patients for OSA within the inpatient setting. As part of this program, the investigators are proposing early access to a sleep apne...
Detailed Description
Currently the standard of care at Lutheran General Hospital for patients does not include a STOP BANG pre-screening assessment, and portable sleep testing (PST) to identify sleep disordered breathing ...
Eligibility Criteria
Inclusion
- • Acute ischemic stroke (AIS) or transient ischemic attack (TIA) diagnosis during hospitalization
- Patient on neurology stroke care unit (10 Tower)
- Consenting adults (≥ 18 years old)
- o For subjects unable to effectively communicate or sign consent due to stroke symptoms, informed consent will be obtained from LAR (legally authorized representative)
- Positive STOP BANG screen
- NIHSS 0-25 (higher NIHSS scores may require application of the PST other than by the patient)
Exclusion
- • Patients who receive sedation within 24 hours of portable sleep testing
- Refusal to sign informed consent
- Non English speaking patient
- Inability to designate Legally Authorized Representative (LAR) for consent
- Participation in other ongoing neurothrombectomy research studies
- Time from symptom onset to emergency department arrival ˃ 72 hours
- Respiratory distress requiring mechanical ventilation or supplemental oxygen at the time of pre screening
- Cardiac or respiratory arrest within past 3 months
- Myocardial infarction (MI) within the past 3 months
- Any unstable medical condition likely to interfere with participation of portable sleep testing
- Life expectancy less than 6 months
- Prior known diagnosis of OSA
- Currently treated with CPAP device
- Pregnant and breastfeeding women
- Prisoners
- Patients unable to complete at least 5 hours of sleep per one night or 8 hours of sleep over 2 nights
Key Trial Info
Start Date :
August 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 31 2019
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT06516354
Start Date
August 1 2017
End Date
March 31 2019
Last Update
October 4 2024
Active Locations (1)
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1
Advocate Lutheran General Hospital
Park Ridge, Illinois, United States, 60068