Application of remifentanil to intravenous sedation in the patients compromised with severe gag reflex
Not Applicable
- Conditions
- gag reflex in dental procedure
- Registration Number
- JPRN-UMIN000025898
- Lead Sponsor
- Depertment of perioperative Medicine, Division of Anesthesiology,Showa University School of Dentistry
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 48
Inclusion Criteria
Not provided
Exclusion Criteria
Exclusion criteria included allergies to remifentanil, fentanyl-related, propofol and midazolam, used than other analgesic drug and sedative drug propofol and remifentanil, ASA class 3 or over, child and disability person.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient and dentist satisfaction by using remifentanil in intravenous sedation
- Secondary Outcome Measures
Name Time Method