Comparison of pain reduction between lidocaine and articaine for anesthesia in extraction of molar teeth
Phase 2
- Conditions
- ocal Anasthesia.Local anaesthetics
- Registration Number
- IRCT2016062627111N2
- Lead Sponsor
- Vice Chancellor for Research, Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 130
Inclusion Criteria
volunteers requiring pulp therapy with intact maxillary molar 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: Patient Self Recall.
- Secondary Outcome Measures
Name Time Method Severity of pain during injection. Timepoint: Immediately after the injection. Method of measurement: Visual analogue pain scale.