irreversible pulpitis.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The exclusion criteria were the presence of systemic disorders, a sensitivity to lidocaine with 1:80,000 epinephrine, a sensitivity to NSAIDs, the presence of widening of the periodontal ligament space, the presence of a periapical radiolucency, lactation, pregnancy. Inclusion criteria included healthy patients having a first mandibular molar tooth with irreversible pulpitis and normal periapical radiographic appearance, whit out spontaneously pain that to be needed emergency treatment.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain degree. Timepoint: Befor and after intervention. Method of measurement: Visual Analogous Scale(VAS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain in the location of injection. Timepoint: 24 and 48 houre after treatment. Method of measurement: Visual analogous scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Kerman University of Medical Sciences