NCT01626989

Evaluation of the Philips Respironics BiPAP autoSV Devices in Subjects With Sleep Disorders

Evaluation of the Philips Respironics BiPAP autoSV Devices in Subjects With Sleep Disorders.

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 44 (actual)
• Sponsor: Philips Respironics · Industry
• Sex: All
• Age: 21 Years – 80 Years
• Healthy volunteers: Accepted

Summary

Comparing two BiPAP autoSV devices in participants with complex sleep apnea and determining if the new device will treat those participants no worse than when compared to its predecessor device.

Detailed description

The use of the BiPAP autoSV4 device in participants with Complex Sleep Apnea Syndrome will treat those participants no worse than when compared to its predecessor device, the BiPAP autoSV Advanced™, with respect to: • Apnea-Hypopnea Index (AHI)

Conditions

• Sleep Disordered Breathing
• Sleep Apnea, Central

Interventions

Type	Name	Description
DEVICE	BiPAP auto Advanced	Auto Servo Ventilation Device
DEVICE	BiPAP auto SV4	Auto Servo Ventilation Device

Timeline

• Start date: 2010-06-01
• Primary completion: 2012-06-01
• Completion: 2012-06-01
• First posted: 2012-06-25
• Last updated: 2019-04-25
• Results posted: 2019-04-25

Locations

3 sites across 1 country: United States