Investigation of respiratory rate measurement by a pulse oximeter during high flow nasal cannula oxygen therapy
Not Applicable
- Conditions
- Respiratory failure
- Registration Number
- JPRN-UMIN000027325
- Lead Sponsor
- The University of Tokyo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 1
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who are not clear consciousness. Patients who are poor pain control. Patients who did not obtain consent. Patients whom investigator judges to be inappropriate as a participant
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of respiratory rate obtained by auscultation and PM 1000 N.
- Secondary Outcome Measures
Name Time Method Comparison of respiratory rate obtained by ECG(thoracic impedance monitor) and PM 1000 N. Comparison of respiratory rate obtained by Capnogram and PM 1000 N.
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie respiratory rate monitoring via pulse oximetry during high flow nasal cannula therapy?
How does pulse oximeter-based respiratory rate measurement compare to standard spirometry in respiratory failure patients?
Are there specific biomarkers that correlate with accurate respiratory rate detection during high flow nasal cannula oxygen therapy?
What are the potential adverse events associated with high flow nasal cannula therapy in respiratory failure patients and how are they managed?
What are the current advancements in pulse oximetry technology for monitoring respiratory parameters in acute respiratory distress syndrome?