NCT00635206View on ClinicalTrials.gov

Investigation of a Novel Positive Pressure Therapy to Rescue Patients Failing to Tolerate CPAP During an Initial Encounter

PHASE3CompletedINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

September 30, 2007

Primary Completion Date

May 31, 2009

Study Completion Date

May 31, 2009

Conditions
Obstructive Sleep Apnea
Interventions
DEVICE

BiPap auto with Fi Flex

"* MinEPAP = 4 cmH2O for prescribed CPAP ≤ 10 cmH2O (use 6 cmH2O for prescribed CPAP \> 10 cmH2O)~* MaxIPAP = 25 cm H2O~* MinPS = 2 cm H2O (cannot be adjusted)~* MaxPS = 8 cm H2O~* Bi-Flex setting of 3"

DEVICE

Standard CPAP

CPAP ≤ 10 cmH2O (use 6 cmH2O for prescribed CPAP \> 10 cmH2O)

Trial Locations (1)

63143

Clayton Slep Institute, St Louis

All Listed Sponsors
lead

Clayton Sleep Insititute

INDUSTRY

NCT00635206 - Investigation of a Novel Positive Pressure Therapy to Rescue Patients Failing to Tolerate CPAP During an Initial Encounter | Biotech Hunter | Biotech Hunter