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OpenTrials
Completed

NCT Number: NCT02364375

Usability Evaluation of Menai CPAP Masks

The primary objective of this study is to evaluate the subjective performance of the Menai mask systems (full face, nasal, and pillows variants), compared against Comparison mask systems.

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

ResMed Sleep Research Centre

Sydney, New South Wales, 2153, Australia

About this study

The study will evaluate the subjective seal, comfort, stability, usability, and humidification performance of the prototype mask systems in CPAP established patients. The performance of the prototype Menai mask systems (full face, nasal, and pillows variants) will be subjectively assessed through user questionnaires based on an 11-point Likert scale, and will be compared against Comparison masks.

The prototype masks share the same parts (cushion, frame, headgear), with the difference being that the Menai masks feature a novel vent and humidification system.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants willing to provide written informed consent
  • Participants who can read and comprehend written and spoken English
  • Participants who are over 18 years of age
  • Participants who have been diagnosed with OSA
  • Participants who have been established on CPAP for ≥ 6 months
  • Participants who are currently using the same mask type/variant as the interventional mask system to be evaluated

Exclusion criteria

  • Participants who are not able to provide written informed consent
  • Participants who are unable to comprehend written and spoken English
  • Participants who are pregnant
  • Participants who are unsuitable to participate in the study in the opinion of the researcher
  • Participants with a pre-existing lung disease or a condition that would predispose them to pneumothorax (e.g. COPD, lung cancer; fibrosis of the lungs; recent (< 2years) case of pneumonia or lung infection, lung injury)
  • Participants who cannot participate for the duration of the trial
  • Participants who are established on bi-level support therapy
  • Participants who are not currently using the same mask type/variant as the interventional mask system to be evaluated

Treatment and study plan

Menai mask (full face)

Device

Prototype mask system (full face variant) with novel vent and humidification system

Menai Standard mask (full face)

Device

Prototype mask system (full face variant) with conventional vent and humidification system

Menai mask (nasal)

Device

Prototype mask system (nasal variant) with novel vent and humidification system

Menai Standard mask (nasal)

Device

Prototype mask system (nasal variant) with conventional vent and humidification system

Menai mask (pillows)

Device

Prototype mask system (pillows variant) with conventional vent and humidification system

Menai Standard mask (pillows)

Device

Prototype mask system (pillows variant) with conventional vent and humidification system

Primary outcomes

  1. Usability Performance Evaluation

    Time frame: 2 weeks

    Evaluation of the usability performance (seal, comfort, etc) of the Menai masks, compared to the Comparison Menai Standard masks.

Secondary outcomes

  1. Humidification Performance Evaluation

    Time frame: 2 weeks

    Evaluation of the humidification performance of the Menai masks (passive humidification), compared to the Comparison Menai Standard masks (active humidification).

Sponsors and collaborators

Lead sponsor

ResMed

Industry

Registry information

Official study title

Menai Mask Systems - Clinical Study 1

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Feb 18, 2015
Registry last updated
Feb 4, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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