Pain Measurement after Root Canal Treatment
Not Applicable
- Conditions
- Asymptomatic Irreversible Pulpitis.Irreversible Pulpitis
- Registration Number
- IRCT201503035141N3
- Lead Sponsor
- Vice chancellor for research, Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 78
Inclusion Criteria
Subjects 20-50 years of age; no systemic diseases; teeth with asymptomatic irreversible pulpitis; normal radiographic periapical appearance.
Exclusion criteria: Subjects under 20 years of age and over 50 years of age; any systemic diseases; nursing and pregnant women; allergies to lidocaine; reversible pulpitis; symptomatic irreversible pulpitis; pulpal necrosis; PDL widening; periapical radiolucency; presence of internal or external resorption; teeth with fixed partial dentures; no bleeding after pulp exposure; use of any analgesics for at least 12 hours before enrollment in the study.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity Postoperative Pain after Root Canal Treatment. Timepoint: at 4-, 12-, 24-, 48- and 72-hour and 1-week after root canal treatment. Method of measurement: Visual Analogue Scale(VAS).
- Secondary Outcome Measures
Name Time Method The Number of Analgesic Tablets Taken. Timepoint: at 4-, 12-, 24-, 48- and 72-hour and 1-week after root canal treatment. Method of measurement: Record by patient.