post operative endodontic pain.
Conditions
Interventions
Intervention 1: "Intervention group1":Nabumetone 750 mg, non steroidal anti-inflammatory drugs prescribe 30 minutes before intervention. Intervention 2: "Intervention group": Nabumetone 500 mg non ste
Sponsors
Tehran Dental Branch, Islamic Azad University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: symptpmatic irreversible pulpitis healthy participants( ASAI &ASAII) first & second molar of maxilla & mandible
Exclusion criteria
Exclusion criteria: systemic disease pregnancy and lactation taking analgesics in the last 12 hours allergic drugs periodontitis & PDLwidening more than 1 mm History of RCT
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain severity. Timepoint: measurement of pain severity before Intervention & 6,12,24,48 hours after finish the Intervention. Method of measurement: heft parker visual analog scale (0_170 mm). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactPeyman Mehrvarzfar
Islamic Azad University
Outcome results
None listed