Evaluation of pulpal anesthesia with articaine
Phase 2
- Conditions
- ocal Anesthesia.Local anaesthetics
- Registration Number
- IRCT201204109367N2
- Lead Sponsor
- Zahedan University of Medical Sciences, Vice-chancellor for Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
patients aged between 18-55 years old who have at least 1 vital first mandibular molar without any restoration or decay
Exclusion criteria: 1.paitients with systemic conditions which eliminate the use of epinephrine. 2.history of allergy to amide anesthetics or contents of local anesthetic cartrige. 3. pregnant women and 4. use of algesics, opioides or any other drugs which influence the anesthesia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Success rate. Timepoint: Each 3 minutes after injection. Method of measurement: With electric pulp tester(EPT).;Onset of anesthesia. Timepoint: Each 3 minutes after injection. Method of measurement: With electric pulp tester(EPT).;Duration of anesthesia. Timepoint: Each 3 minutes after onset of anesthesia. Method of measurement: With electric pulp tester(EPT).
- Secondary Outcome Measures
Name Time Method