Extracting the mandibular double-sided wisdom teeth.
Conditions
Interventions
In this double-blind clinical trial, anti-inflammatory and anti-inflammatory effects of topical administration of a 20% tissue bioadhesive made of 100% ginger extract and a mucosal dexamethasone injec
Treatment - Drugs
Sponsors
The Vice-Chancellor of Research of Bushehr University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Inclusion criteria: The patient has a double-walled tooth (based on the angle of tooth placement in the jaw, the amount of bone and soft tissue on the tooth, the condition of the tooth in relation to the anterior border of ramus), the willingness to cooperate And there is no prohibition of tooth surgery or sensitivity to ginger. The tooth does not have any pathological lesions in the root zone in clinical and radiographic examinations. No other surgical procedures for at least two weeks. Exclusion criteria: kidney or liver disease, bleeding problems such as hemophilia, neutropenia, blood platelet deficiency, etc., previous or current stomach ulcers, any heart disease, Known allergies, allergies, or individual reactions to either the drugs used or the drugs that may be used in the study (ginger, lidocaine anesthesia, acetaminophen codine 300, gelofen 400, amoxicillin 500, and metronidazole 400 mg G) Pregnancy and lactation, taking analgesic or anti-inflammatory drugs 24 hours before the study, having pain and other inflammatory symptoms including swelling, high blood pressure and the inability to open the mouth before the study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The amount of pain. Timepoint: Day of intervention, one day after intervention, two days after intervention, three days after intervention. Method of measurement: VAS scale (number).;Mouth opening rate. Timepoint: Pre-intervention, 24 hours after intervention, 72 hours after intervention. Method of measurement: Millimeters.;Distance between the corner of the mouth and the tragus. Timepoint: Pre-intervention, 24 hours after intervention, 72 hours after intervention. Method of measurement: Millimeters.;The amount of acetaminophen codoine 300 mg taken. Timepoint: Day of intervention, one day after intervention, two days after intervention, three days after intervention. Method of measurement: questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Age. Timepoint: Before intervention. Method of measurement: questionnaire.;Gender. Timepoint: Before intervention. Method of measurement: questionnaire.;Infection. Timepoint: Before intervention, 24 hours after intervention, 72 hours after intervention. Method of measurement: View, interview.;Any other anti-inflammatory or analgesic drug. Timepoint: three days after the intervention. Method of measurement: questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSahar Zandi
School of Dentistry, Bushehr University of Medical Sciences
Outcome results
None listed