comparison of anesthetic effect between lidocaine and articai
Phase 4
- Conditions
- local anesthesia.Local anaesthetics
- Registration Number
- IRCT2015110613932N3
- Lead Sponsor
- Vice Chancellor for Research, Hormozgan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 16
Inclusion Criteria
healthy volunteers with intact maxillary central incisor that response to pulp tester; individuals who can use visual analogue pain scale
Exclusion criteria: patients with periodontal disease; positive history of alcohol consumption; cigarette smoking; drug user; patients who have received antidepressant or steroid analogues drug during the 48 hours before study; pregnant patients; patients with known allergy to lidocaine or epinephrine; peripheral neuropathy, positive history of dental phobia or any damage to teeth
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset time of anesthesia. Timepoint: 1 minute intervals. Method of measurement: Electric Pulp Test.;Severity of pain during injection. Timepoint: Immediately after the injection. Method of measurement: Visual analogue pain scale.
- Secondary Outcome Measures
Name Time Method