Post dental surgery pain. Other acute postprocedural pain
Conditions
Interventions
Intervention 1: Intervention group: subjects receive a mixture of Bupivacaine 0.5% (1.8 ml) with epinephrine 1:200000 (Novocal Pharmucautical of Canada Inc. Cambridye, Ontario N1R6) and 0.5 mg/kg Dexm
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: Patients with impacted wisdom tooth (Mesioangular, class II B in Pel and Gregory classification) 18 to 30 years old ASA I status Referred to Shahid Beheshti Dental School for Surgery and willing to be enrolled in the study
Exclusion criteria
Exclusion criteria: Patients who receive psychological drugs or have drug addiction More than one tooth surgery or other dental treatments such as root canal therapy Impact tooth in other categories of Pel and Gregory classification Refuse to study enrollment Women in menses
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post surgical pain. Timepoint: 4, 8, 12 hours after surgery. Method of measurement: The pain severity is measured using visual analogue scale by asking patients: 0-10 (0-3 mild, 4-6 moderate and 7-10 sever which subjects need pain relief drugs).;The amount of analgesics that is used by patients. Timepoint: Consumption of analgesic within 12 hours after surgery. Method of measurement: Asking patients. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactPegah Mehrabi Nia
Shahid Beheshti University of Medical Sciences
Outcome results
None listed