Bipap autoSV Advanced in Central Apnea Patients

Status Completed

Clinical Trial Summary

Pilot study testing the Bipap autoSV Advanced Algorithm during full night, in-lab PSG and 3 months at home on patients with Central Sleep Apnea, Hunter Cheyne Stokes Respiration, or Complex Sleep Apnea.

Clinical Trial Description

Participants who qualify will be scheduled for one full night, attended diagnostic PSG, one full night attended CPAP titration, and one full night attended BiPAP autoSV Advanced titration PSG. Participants will be provided a BiPAP autoSV Advanced to use at home for 90 days. ;

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01199042
Study type	Interventional
Source	Philips Respironics
Contact
Status	Completed
Phase	N/A
Start date	September 2010
Completion date	May 2013

View Details

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