In-Hospital Portable Sleep Monitoring for the Evaluation of Obstructive Sleep Apnea (OSA)
This trial is active, not recruiting.
|Condition||obstructive sleep apnea|
|Treatment||testing with a portable sleep apnea monitor .|
|Sponsor||John H. Stroger Hospital|
|Start date||April 2011|
|End date||February 2015|
|Trial size||140 participants|
|Trial identifier||NCT01424592, CCHHS IRB 11-027|
Hypothesis: Portable sleep testing of hospitalized medical inpatients suspected of having OSA is accurate in determining the need for positive airway pressure (PAP) therapy when compared to outpatient laboratory-based polysomnography.
- Hospitalized medical inpatients referred for suspected OSA will be tested with a portable sleep apnea testing device during hospitalization.
- These patients will then undergo an outpatient laboratory-based attended polysomnography after hospital discharge.
- Results of the inpatient portable sleep apnea test will be compared to the outpatient laboratory-based polysomnography in terms of diagnostic accuracy.
Male or female participants at least 18 years old.
Inclusion Criteria: - Hospitalized inpatients referred for evaluation of suspected obstructive sleep apnea Exclusion Criteria: - Patients admitted to surgical or obstetrics/gynecology services - Patients with certain medical conditions (altered mental status not related to respiratory failure, septicemia, unstable psychiatric disorder, narcotic abuse and prior diagnosed sleep apnea) - Patients with certain social histories (prisoners) - Patients unable to use CPAP (facial deformity and traumatic facial injuries).
|Official title||Inpatient Portable Sleep Apnea Testing of Hospitalized Medical Patients for the Evaluation of Obstructive Sleep Apnea Prospectively Compared to Outpatient Laboratory-based Polysomnography|
|Principal investigator||Swamy Nagubadi, MD|
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