Comparison of dexmedetomidine and propofol for conscious sedation in dental surgery
Phase 4
- Conditions
- adult patients who need intravenous sedation for dental surgery
- Registration Number
- JPRN-UMIN000013448
- 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
- 88
Inclusion Criteria
Not provided
Exclusion Criteria
patients aged over 80; ASA physical status 3 and 4; patients with contraindications to propofol, dexmedetomidine and midazolam; allergy to soybean or egg; a history of cardiovascular or respiratory disease; use of drugs for psychotropic and cardiac desease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method unexpected patient movements
- Secondary Outcome Measures
Name Time Method responsiveness, mouth opening time, cough reflex, snoring, total and rescue dose of midazolam, patient and operator satisfaction, memory of the procedure, recovery behaviour after sedation.