Study of the local-anesthetic-effect time and the range of a lidocaine with epinephrine
Not Applicable
- Conditions
- A healthy volunteer without a sickness
- Registration Number
- JPRN-UMIN000008969
- Lead Sponsor
- Department of Dental Anesthesiology Faculty of Dental Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 18
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Those who have an allergy in a local anesthetic (2) Those who have a sickness of the circulatory system (3) Those who have a sugar diabetes (4) Those who have a toxic goiter (5) Those who have serious hepatic function disorder and renal impairment (6) In addition, those who judged that a test doctor in attendance was unsuitable
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method It is each test solution 1 mL to the root-tip equivalent part gingival of a left-side up-and-down jaw fang.Until it recovers the range in every 10 minutes from an operation using the 2-point-discrimination method of transfusion .6 mm on the same level as record . 2-hour and 30 minutes, or perception's time until sense of pain of labia oris is recovered by record . Pinprick method study-before by a side periosteum narcosis,It recorded, the front masque photography was taken at the time of the termination of termination ., and the variation of the range was evaluated based on marking at the time of each measure.
- Secondary Outcome Measures
Name Time Method