sing of the absorbable scaffold containing slow releasing lidocaine in surgery area.
Not Applicable
- Conditions
- Impacted teeth.An impacted tooth is a tooth that has failed to erupt because of obstruction by another tooth.
- Registration Number
- IRCT201705063018N3
- Lead Sponsor
- Research Vice-chancellor Tabriz Univercity of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 72
Inclusion Criteria
third molars teeth surgery in patients with bone impaction.
Exclusion criteria: for patients with sinoatrial bluck heart disease and those who have adams stokes syndrom and wolff parkinson white syndrom; those taking the following drugs: quinidine, disopiramid, procainamide Amiodarone hydrochloride and are treated with caution in these patients: elderly patients; porphyrya; hepatic failure; bradycardia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Determination and comparison of pain levels in the control and placebo groups of slow-releasing lidocain as scaffolds in the surgical area of the impacted wisdom teeth. Timepoint: Immediately after surgical intervention. Method of measurement: visual analog scale way.
- Secondary Outcome Measures
Name Time Method Determination and comparison of the onset time of pain in the control and placebo groups of the slow-releasing lidocaine as a scaffold in the surgical area of the impacted wisdom teeth. Timepoint: Immediately after surgical intervention. Method of measurement: In the checklist, the time of the onset of pain and the duration of the pain are asked verbally from the patient and within a few hours the patient's response will be recorded.