The socket caused by impacted wisdom tooth surgery.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged 18 to 25 years With Impacted third Mandibular Molars Without Pericoronitis or Infection Who are not Pregnant Have no life-threatening Systemic Disease No Allergy to the Drugs used in the Study No recent use of Antibiotics or Anti-inflammatory Drugs Who are willing to participate in the Study
Exclusion criteria
Exclusion criteria: Those whose Follow-up for recording Pain and Swelling was not possible Who were unwilling to continue in the Study Individuals whose Healing process was not normal Patients who used other Anti-inflammatory Drugs or Antibiotics after Surgery Whose Impacted third Molars were located close to the Nerve Canal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain severity. Timepoint: The 2nd, 4th, and 7th Days After Surgery. Method of measurement: The Visual Analogue Scale will be used to measure the severity of patients' pain. The patient will be given a ten-centimeter ruler, numbered from 0 to 10, and the patient must indicate the level of pain on it on the second, fourth, and seventh days. | — |
Secondary
| Measure | Time frame |
|---|---|
| Facial swelling. Timepoint: The 2nd, 4th, and 7th days after surgery. Method of measurement: To measure swelling, we measure from the outer canthus of the eye to the mandibular protuberance, from the middle of the tragus of the ear to the outer corner of the lip on the same side in millimeter.;Trismus severity. Timepoint: The 2nd, 4th, and 7th days after surgery. Method of measurement: We measure the distance between the edges of the upper and lower incisors in millimeters. | — |
Countries
Iran (Islamic Republic of)
Contacts
Khoram-Abad University of Medical Sciences