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RespirAq Humidifier Usability During Invasive Ventilation

NCT04765878 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2021-03-10

No results posted yet for this study

Summary

This study aims to capture preliminary safety and effectiveness information on a near-final humidifier device design and to provide data for more extensive research, if required. This feasibility study will investigate the following: process, resources, management, and scientific aspects of delivering humidification by the RespirAq humidifier device in ventilated patients.

Conditions

  • Mechanical Ventilation

Interventions

DEVICE

RespirAq Humidification

Humidifier

Sponsors & Collaborators

  • Ministry of Business, Innovation and Employment

    collaborator UNKNOWN

  • Waikato District Health Board

    collaborator UNKNOWN

  • Auckland University of Technology

    lead OTHER

Principal Investigators

  • Melanie Moylan · Auckland University of Technology

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-31
Primary Completion
2021-04-30
Completion
2021-04-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04765878 on ClinicalTrials.gov