pain. Atypical facial pain
Conditions
Interventions
Intervention 1: Control group: It is Normal saline and patients in the control group are asked to rinse their mouth twice a day for 15 days after surgery with the normal saline. Intervention 2: First
Sponsors
Zahedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: It has a wisdom tooth in the mandible with a degree of secrecy of levels A and B and classes I and II (based on the Pell & Gregory classification). Age between 18 and 50 years Conscious consent to participate in the study It has commuting and follow-up facilities after intervention
Exclusion criteria
Exclusion criteria: Any systemic disease Patients who experience severe pain or abscesses after surgery and are unable to attend the follow-up session. Patients whom surgery has been performed traumatized
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The amount of pain. Timepoint: Right before surgery,One day, three days, seven days, fifteen days after taking the gel will be done twice a day. Method of measurement: The patient's pain measurement will be on Visual analog scale (VAS).;Amount of swelling. Timepoint: Right before surgery,One day, three days, seven days, fifteen days after taking the gel will be done twice a day. Method of measurement: The linear distance between the lingual surface of the first molar mandibular and the tangent to the skin of the cheek is measured using a caliper. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSina Hakimi
Zahedan University of Medical Sciences
Outcome results
None listed