Comparing the effect of supplementary injection on inferior alveolar nerve block success rate
Not Applicable
- Conditions
- irriversible pulpitis.
- Registration Number
- IRCT2015112715782N3
- Lead Sponsor
- investigator
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 160
Inclusion Criteria
patients between 18 to 65 years old; without any systematic disease or drug using; no allergic reaction to the anesthetic; no smoking; not using analgesic 24 hours ago; no pregnant or breastfeeding and they must have one molar with irreversible pulpitis.
Exclusion criteria: pulp necrosis; periapical radioluscency.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 15 minute after injection. Method of measurement: Heft Parker visual analog scale.
- Secondary Outcome Measures
Name Time Method