Nexus Compliance Study

NACompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

November 30, 2009

Primary Completion Date

March 31, 2010

Study Completion Date

April 30, 2010

Conditions
Obstructive Sleep Apnea
Interventions
DEVICE

CPAP Pre Nexus (S9)

This is the patient's own CPAP prior to trialling the Nexus (S9). 4 weeks of data will be downloaded from this device and compared to 4 weeks using Nexus (S9), and 4 weeks usage post trialling Nexus (S9)

DEVICE

Nexus (S9)

The patient will use the new Nexus (S9) CPAP for four weeks in place of their usual CPAP every night when they sleep to treat their OSA. Compliance data will be compared between four weeks on this device to the last four weeks on their current device (CPAP Pre S9). After using the Nexus (S9) CPAP for four weeks, participants will return to their current device for four weeks. Data from this post-trial period will be compared with both the Nexus (S9) four weeks, and the four weeks pre Nexus (S9) usage.

DEVICE

CPAP Post Nexus (S9)

After trialling the Nexus (S9) for four weeks, patients will return to their usual CPAP. Data from the patient's usual CPAP for four weeks will be compared to data while using the Nexus (S9), and data from the patient's usual device pre trialling S9 (CPAP Pre Nexus)

Trial Locations (1)

2153

ResMed Sleep Reseach Centre, Sydney

Sponsors

Lead Sponsor

All Listed Sponsors
lead

ResMed

INDUSTRY

NCT01013207 - Nexus Compliance Study | Biotech Hunter | Biotech Hunter