Comparison of recovery time after intravenous sedation using dexmedetomidine in combination with propofol or midazolam
Not Applicable
- Conditions
- Require dental procedure under intravenous sedation
- Registration Number
- JPRN-UMIN000039668
- 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
- 54
Inclusion Criteria
Not provided
Exclusion Criteria
1. A history of allergic reactions to the drugs used in this study 2. Allergic reaction to yolk and soy 3. Hepatic or renal dysfunction 4. Maternal and nursing women 5. Circulatory or respiratory dysfunction 6. Acute narrow-angle glaucoma 7. Myasthenia gravis 8. Receiving HIV protease inhibitors or HIV reverse transcriptase inhibitors 9. Prescribed antipsychotics 10. brain disorder 11. Severe obesity, micrognathia, tonsillar hypertrophy, sleep apnea syndrome
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time from the end of the sedatives administration until the Romberg test is successfully performed.
- Secondary Outcome Measures
Name Time Method Time from the end of the sedatives administration until achieving an Aldrete score of 9 or 10. Time from the end of the sedatives administration until patients possible to sit. Time from the end of the sedatives administration until patients possible to stand up.