Intubation Assist Clinical Study
Completed
- Conditions
- Intubation, Intratracheal
- Registration Number
- NCT03301324
- Lead Sponsor
- Zoll Medical Corporation
- Brief Summary
The Intubation Assist Clinical Study is an observational study of adult patients scheduled for elective surgery under general anesthesia to assess the user interface, assess transthoracic impedance by the ventilation volume and assess transthoracic impedance. Monitoring will begin at the time the patient is pre-oxygenated in preparation for endotracheal intubation and will continue until 30 minutes after intubation is achieved.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
- 18 years of age or older
- Requiring intubation and assisted ventilation
- Patient undergoing elective surgery
- Able to give informed consent
Exclusion Criteria
- Skin condition that would interfere with electrodes
- Inability/failure to intubate
- Pregnancy
- Surgery that prevents the application of electrodes and monitoring equipment.
- Previous excision of complete or partial lung; congenital lung abnormalities.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of the user interface Assessment will be made after using Intubation Assist approximately 30 minutes after successful intubation
- Secondary Outcome Measures
Name Time Method Assessment of transthoracic impedance Impedance measurements will be collected during intubation and will not exceed 30 minutes from the start of intubation
Trial Locations
- Locations (1)
Oslo University Hospital
🇳🇴Oslo, Norway