Pain after root canal therapy. Pulpitis
Conditions
Interventions
Intervention 1: Control group:Half of the samples receiving acetaminophen 500 mg and placebo every 6 hours until the pain improved and their pain before treatment, 24, 12, 6 and 48 hours after treatme
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
10 Years to No maximum
Inclusion criteria
Inclusion criteria: The age range of all patients be 10 years and older tooth Periapical tissue be normal
Exclusion criteria
Exclusion criteria: Pregnant women do not enter the study Patients who have kidney and coagulation problems Patients taking anticoagulants patient has a systemic problem
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Score in Visual Analog Scale System (VAS). Timepoint: Before treatment and 6,12,24and 48hours after treatment. Method of measurement: Visual analog scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of the effecacy of bromelaine in reduce postoperative pain following root canal therapy secondary consequences can be a pain reduction score. Timepoint: To measure pain befor root canal therapy , 6 ,12 ,24 and 48 hours after root canal therapy is used . Method of measurement: Evaluation of the effecacy of bromelaine in reduce postoperative pain following root canal therapy secondary consequences pain reduction score Visual Analogue Scale can be used . | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Abbasi
Esfahan University of Medical Sciences
Outcome results
None listed