Clinical Trials Directory

Trials / Terminated

TerminatedNCT00588848

CPAP vs AutoCPAP for Treatment of Obstructive Sleep Apnea (OSA) in the Postoperative Setting

Postoperative Management of Obstructive Sleep Apnea With CPAP vs. an Autoadjusting CPAP Device: a Randomized Controlled Single Center Trial

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
11 (actual)
Sponsor
MetroHealth Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if an Autoadjusting CPAP machine is better than the regular CPAP machine in treatment of Obstructive Sleep Apnea in the postoperative setting.

Detailed description

The purpose of this study is to determine if an Autoadjusting CPAP machine is better than the regular CPAP machine in treatment of Obstructive Sleep Apnea in the postoperative setting. Patients with known Obstructive Sleep Apnea who are on CPAP therapy at home and undergo an elective surgery (meeting specified inclusion and exclusion criteria) will be randomized to either using Autoadjusting CPAP vs their usual CPAP at their prescribed settings the night after surgery. During that night, they will be monitored with full polysomnography in their hospital bed.

Conditions

Interventions

TypeNameDescription
DEVICEAutoadjusting CPAP (VPAP Auto)An autoadjusting CPAP unit is used in place of subject's own CPAP unit during the night of the polysomnography study (the first night after surgery).
DEVICECPAPSubject's own CPAP unit is applied to the subject during the polysomnography study night (the first night after surgery)

Timeline

Start date
2008-01-01
Primary completion
2011-04-01
Completion
2011-04-01
First posted
2008-01-09
Last updated
2019-01-14
Results posted
2013-05-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00588848. Inclusion in this directory is not an endorsement.