Impacted teeth. An impacted tooth is a tooth that has failed to erupt because of obstruction by another tooth.
Conditions
Interventions
Intervention 1: In the 24 patients of the intervention group, will used absorbable scaffold of lidocaine in the surgery area. Intervention 2: 24 other patients of the placebo group will be usining emp
Treatment - Surgery
Placebo
Treatment - Drugs
In the 24 patients of the intervention group, will used absorbable scaffold of lidocaine in the surgery area.
24 other patients of the placebo group will be usining empty scaffolds without lidocaine.
In 24 of the control group, post-operative routine analgesic treatments (staggel 500 mg and 400 mg jelly) are used and no other therapeutic intervention will be taken.
Sponsors
Research Vice-chancellor Tabriz Univercity of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: 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
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNadiyeh Abdolahyazar
Tabriz University of Medical Sciences
Outcome results
None listed