At a glance
ClinicalIndex Comparison RecordN/ACompleted· 20 enrolled
Drug / intervention
PSIdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Propofolsleep - A Observational Study on Cardiopulmonary and Pharyngeal Reactions While Drug Induced Sleep Endoscopy in Patients With Obstructive Sleep Apnea Syndrome Under PSI Monitoring
In Brief
An observational study evaluating PSI for Sleep Apnea, Obstructive and 4 related conditions. Completed, enrolled 20 participants across 1 site.
Detailed Summary
While Drug Induced Sleep Endoscopy (DISE) in patients with obstructive sleep apnea syndrome (OSAS) apnea and hypopnea occur. Because of the induced phases of apnea in a controlled setting it is possible to evaluate the related pathophysiology of apnea. We plan to correlate the Patient State Index (PSI) and other physiologic parameters with phases of apnea and hypopnea.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsSleep Apnea, Obstructive, Electroencephalography, Echocardiography, Blood Gas Monitoring, Transcutaneous, Consciousness Monitors
CountriesGermany
Collaborators--
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
First PostedJul 2017
Enrollment StartAug 2017
Primary CompletionOct 2019
Study CompletionDec 2019
TodayJul 2026
First PostedJul 21, 2017
Enrollment StartAug 22, 2017
Primary CompletionOct 30, 2019
Study CompletionDec 31, 2019
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 8.9 years ago
Interventions
PSIdevice
The PSI delivered by Masimo Root (Sedline) will be measured in all patients.