Study of analgesic and anti-inflammatory effect of ginger
- Conditions
- Extracting the mandibular double-sided wisdom teeth.
- Registration Number
- IRCT2017082635906N1
- Lead Sponsor
- The Vice-Chancellor of Research of Bushehr University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
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.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.