CPAP Device In-lab Assessment NZ

Summary

The purpose of this trial is to assess device performance against participants in an overnight study to ensure the product meets user and clinical requirements

Conditions

• Obstructive Sleep Apnea

Interventions

DEVICE

Auto CPAP + comfort feature A

Auto CPAP + comfort feature A using Fisher \& Paykel Healthcare CPAP Device

DEVICE

Auto CPAP with comfort feature B

Auto CPAP with comfort feature B using Fisher \& Paykel Healthcare CPAP Device

DEVICE

Auto CPAP with no comfort feature

Auto CPAP with no comfort feature using Fisher \& Paykel Healthcare CPAP Device

DEVICE

Auto CPAP with comfort feature A+B

Auto CPAP with comfort feature A+B using Fisher \& Paykel Healthcare CPAP Device

DEVICE

CPAP with comfort feature A

CPAP with comfort feature A using Fisher \& Paykel Healthcare CPAP Device

DEVICE

CPAP with comfort feature B

CPAP with comfort feature B using Fisher \& Paykel Healthcare CPAP Device

DEVICE

CPAP with no comfort feature

CPAP with no comfort feature using Fisher \& Paykel Healthcare CPAP Device

DEVICE

CPAP with comfort feature A + B

CPAP with comfort feature A + B using Fisher \& Paykel Healthcare CPAP Device

DEVICE

CPAP at Sub therapeutic level

CPAP at Sub therapeutic level using Fisher \& Paykel Healthcare CPAP Device

Sponsors & Collaborators

• Fisher and Paykel Healthcare

  lead INDUSTRY

Study Design

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Model

CROSSOVER

Eligibility

Min Age

18 Years

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2016-11-30

Primary Completion

2017-03-31

Completion

2017-03-31

Countries

• New Zealand

Study Locations