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Measurement of PPG waveforms for Obstructive Sleep Apnea
N/A
Waitlist Available
Research Sponsored by Sotera Wireless, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients twenty-one years of age or older
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 - 8 hours
Awards & highlights
Study Summary
The goal of this study is to collect raw waveform data for two separate noninvasive methods, both of which may be useful for the assessment of upper airway obstruction.
Eligible Conditions
- Obstructive Sleep Apnea
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 - 8 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 - 8 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Measurement of pulse arrival time in patients with obstructive sleep apnea syndrome.
Secondary outcome measures
Non-invasive Photoplethysmographic (PPG) measurement in patients with obstructive sleep apnea syndrome.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Measurement of Pulse Arrival Time (PAT)Experimental Treatment1 Intervention
Collection of PAT waveform data from patients with obstructive sleep apnea for 4-8 hours
Group II: Measurement of PPG waveformsExperimental Treatment1 Intervention
Collection of photoplethysmograph(PPG)waveform data from patients with obstructive sleep apnea for 4-8 hours
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Who is running the clinical trial?
Sotera Wireless, Inc.Lead Sponsor
2 Previous Clinical Trials
165 Total Patients Enrolled
James Welch, MSStudy DirectorSotera Wireless
Frequently Asked Questions
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