Study on the efficacy and safety of lidocaine tape application as a surface anesthesia for the mucous membranes of the mouth
- Conditions
- Healthy volunteers
- Registration Number
- JPRN-jRCTs061230003
- Lead Sponsor
- Yanamoto Souichi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 14
1. Age: 18 years old or older and under 60 years old at the time of obtaining consent.
2. Gender: Any gender
3. Persons who have no inflammation or other abnormal findings in the area to which the study drug will be applied (mucosa of the maxillary lateral incisor in the vestibular region of the oral cavity).
4.Persons who have received a thorough explanation of their participation in this study, and who have given their free and voluntary written consent based on a thorough understanding.
1. Persons who are judged to lack the ability to make decisions regarding participation in this study.
2. Persons who are allergic or hypersensitive to any of the drugs in this study
3. Persons with drug sensitivity who are allergic to dental Xylocaine cartridges.
4. Pregnant women or women who may be pregnant.
5. Persons with relevance to the department of Oral and Maxillofacial Surgery, Hiroshima University Hospital
6. Any other person who is deemed inappropriate as a research subject by the principal investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method