RespirAq Humidifier Usability During Invasive Ventilation
Not Applicable
- Conditions
- Mechanical Ventilation
- Interventions
- Device: RespirAq Humidification
- Registration Number
- NCT04765878
- Lead Sponsor
- Auckland University of Technology
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 20
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Humidification RespirAq Humidification -
- Primary Outcome Measures
Name Time Method Temperature max 24 hours Meet ISO standard
Humidity max 24 hours Meet ISO standard
- Secondary Outcome Measures
Name Time Method