Effect of combination of intravenous propofol and inhaled nitrous oxide: a randomized clinical trial
Not Applicable
- Conditions
- healthy adult volunteers
- Registration Number
- JPRN-UMIN000009728
- Lead Sponsor
- Osaka University Graduate School of Dentistry
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 26
Inclusion Criteria
Not provided
Exclusion Criteria
A history of cardiovascular disease, hypertension, respiratory disease and dysautonomia were considered criteria for exclusion from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hemodynamics, heart rate variability, depth of sedation
- Secondary Outcome Measures
Name Time Method