RespirAq Humidifier Usability During Invasive Ventilation

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-31

Study Completion Date

2021-04-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Mechanical Ventilation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Humidification

Group Type EXPERIMENTAL

RespirAq Humidification

Intervention Type DEVICE

Humidifier

Interventions

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RespirAq Humidification

Humidifier

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

Patients scheduled for coronary artery bypass surgery (CABG) will be recruited before their surgical procedure at the Waikato district health board during February, March, and April of 2021.

Exclusion Criteria

* Age \<18 years
* Have any other condition which, at the investigator's discretion, is believed may present a safety risk or impact the feasibility of the study or the study results
* Patients admitted for emergency CABG surgery
* Unable to provide written informed consent before surgery
* Patients who would be contra-indicated to HME humidification devices

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No