efficacy of premedication on success rate of anesthesia in lower jaw
Phase 2
- Conditions
- Irriversible pulpitis.Irriversible pulpitis
- Registration Number
- IRCT2015071423207N1
- Lead Sponsor
- Research deputy, Dentsal School, Shahid Beheshti University of Medical Schiences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 92
Inclusion Criteria
patients with the signs and symptoms of irreversible pulpitis in mandibular first molar tooth.
Exclusion criteria: presence of any systemic diseases; pregnancy or breast-feeding; taking any kind of medications within a period of 8 h prior to the treatment that could interfere with the medications used in this study; teeth with extensive coronal restorations; casting restorations; previous root canal therapies; severe periodontal diseases and peri apical radiolucencies; and contraindications to the drugs used in this study
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tooth sensitivity. Timepoint: before intervention and one hour after intervention. Method of measurement: using EPT device.;Pain level. Timepoint: before intervention and one hour after intervention. Method of measurement: using Heft Parker visual analog scale.
- Secondary Outcome Measures
Name Time Method