A research for the application of pregabalin for anesthesia and interaction of pregabalin and anesthetic agent
Not Applicable
- Conditions
- condition which needs operation under anesthesia
- Registration Number
- JPRN-UMIN000015674
- Lead Sponsor
- Faculty of Dental Science, Kyushu University, Department of Dental Anesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
Volunteers were excluded from recruitment if they were allergic to egg, soy and milk, allergic to any antibiotics or painkiller, chronic neuralgia patients, taking any GABA derivatives, or had dental disease that might cause severe pain
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood concentration of propofol to acheive the sufficient sedative level during intravenous sedation
- Secondary Outcome Measures
Name Time Method Circulation and respiration dynamics during intravenous sedation, perioperative analgesic effect, first propofol injection-induced pain and side effects at 30 minutes and 1hour after pregabalin administration, and 30 minutes. 1 hour and 5 hour after the intravenous sedation end.