Comparison of two oral analgesic pre-medication on success of intraoral anesthesia
Phase 2
Completed
- Conditions
- Irreversible pulpitis.
- Registration Number
- IRCT2015081116845N3
- Lead Sponsor
- Vice Chancellor of Research ,Dental Branch Islamic Azad University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
patients with age ranged 18-65; without systemic diseases ; without any medicine consumption; non smoking; non pregnant; non breast feeding; with asymptomatic irreversible pulpitis ( Visual Analog Scale = 54); no allergies and hypersensitivity history to Non-steroidal anti-inflammatory drugs and acetaminophen; need root canal treatment for a mandibular molar
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anesthesia following the injection. Timepoint: 5 minutes. Method of measurement: Electric pulp tester.
- Secondary Outcome Measures
Name Time Method Root Canal treatment without pain. Timepoint: 15 minutes following injection. Method of measurement: Pain rate based on VAS.