None listed
Conditions
Interventions
Intervention 1: Intervention group: Intervention group 1: Patients receiving novafen (acetaminophen 325 mg, ibuprofen 200 mg and caffeine 40 mg, Elahi Medical Company, Iran) after surgery. Interventi
Sponsors
Islamic Azad University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Bilateral candidate for mandibular third molars Having informed consent to enter the study
Exclusion criteria
Exclusion criteria: Having systemic disease Having local infections such as pericoronitis Smoking History of taking oral contraceptives during the last 4 weeks Poor oral health Pregnancy Allergy to pineapple and plant compounds Having coagulation problems Use of other drugs during the study period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Trismus, pain and swelling. Timepoint: Before surgery, one and three days after surgery. Method of measurement: Patients' pain using visual analog classification criteria (0 indicates no pain and 10 indicates maximum pain), swelling by measuring the corner of the mouth to the connection of the ear lobe following the protrusion of the cheek and the degree of trismus by measuring the intercostal distance using a The ruler is measured and the results are reported in millimeters. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZabihullah Mohaghegh
Birjand University of Medical Sciences
Outcome results
None listed